EPINEPHRINE EPINEPHRINE

EPINEPHRINE 10 ml Injection

HOSPIRA, INC. FDA Rx Only

Epinephrine Injection USP, 1 mg/10 mL (0.1 mg/mL) is supplied as a sterile aqueous solution with a pH range of 2.3–3.5, that is clear, colorless, and nonpyrogenic. Each milliliter contains 0.1 mg epinephrine, 8.16 mg sodium chloride, 0.46 mg sodium metabisulfite, and 2.13 mg citric acid, anhydrous and 0.41 mg sodium citrate, dihydrate added as buffers. Additional citric acid and/or sodium citrate may be added for pH adjustment. The solution contains no preservatives. This sterile solution is to be administered after dilution by the intravenous route. Epinephrine is a sympathomimetic catecholamine (adrenergic agent) designated chemically as 4-[1-hydroxy-2 (methylamino) ethyl]-1,2 benzenediol, a white, crystalline powder. It has the following structural formula: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Chemical Structure

epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

SPORTPHARM LLC FDA Rx Only

Epinephrine injection, USP 0.3 mg is an auto-injector and a combination product containing drug and device components. Each epinephrine injection, USP 0.3 mg delivers a single dose of 0.3 mg epinephrine from epinephrine injection, USP (0.3 mL) in a sterile solution. Epinephrine injection, USP 0.3 mg contain 1.1 mL of epinephrine solution. 0.3 mL epinephrine solution is dispensed for epinephrine injection, USP 0.3 mg, when activated. The solution remaining after activation is not available for future use and should be discarded. Each 0.3 mL in epinephrine injection, USP 0.3 mg contains 0.3 mg epinephrine, 2.6 mg sodium chloride, not more than 1.5 mg chlorobutanol, 0.45 mg sodium bisulfite, hydrochloric acid and sodium hydroxide to adjust pH, and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace epinephrine injection, USP if the epinephrine solution appears discolored (pinkish or brown color), cloudy, or contains particles. Thoroughly review the patient instructions and operation of epinephrine injection, USP with patients and caregivers prior to use [see Patient Counseling Information ( 17 ) ]. Chemical Structure

EPINEPHRINE EPINEPHRINE

EPINEPHRINE 10 ml Injection

HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

Epinephrine Injection USP, 1 mg/10 mL (0.1 mg/mL) is supplied as a sterile aqueous solution with a pH range of 2.3–3.5, that is clear, colorless, and nonpyrogenic. Each milliliter contains 0.1 mg epinephrine, 8.16 mg sodium chloride, 0.46 mg sodium metabisulfite, and 2.13 mg citric acid, anhydrous and 0.41 mg sodium citrate, dihydrate added as buffers. Additional citric acid and/or sodium citrate may be added for pH adjustment. The solution contains no preservatives. This sterile solution is to be administered after dilution by the intravenous route. Epinephrine is a sympathomimetic catecholamine (adrenergic agent) designated chemically as 4-[1-hydroxy-2 (methylamino) ethyl]-1,2 benzenediol, a white, crystalline powder. It has the following structural formula: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. STRUCTURE

Epinephrine EPINEPHRINE

EPINEPHRINE 10 ml Injection

MEDICAL PURCHASING SOLUTIONS, LLC FDA Rx Only

Epinephrine, USP is a non-selective alpha and beta-adrenergic agonist designated chemically as (R) -4-(1-Hydroxy-2-(methylamino)ethyl)benzene-1,2-diol, a white, microcrystalline powder. It has the following structural formula: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Epinephrine Injection USP, 1 mg/10 mL (0.1 mg/mL) is supplied as a sterile aqueous solution that is clear, colorless and nonpyrogenic. Each mL of the solution contains epinephrine (0.1 mg) as the active ingredient and the following inactive ingredients: citric acid monohydrate (3.3 mg), edetate disodium dihydrate (0.004 mg), sodium chloride (8.2 mg), sodium citrate dihydrate (1.5 mg), sodium metabisulfite, and Water for Injection. Hydrochloric acid solution is added to dissolve the active ingredient. Sodium hydroxide solution is added to adjust the pH. Nitrogen is used for blanketing protection. Solution must be diluted prior to intravenous use. structure

Epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

TEVA PHARMACEUTICALS USA, INC. FDA Rx Only

Epinephrine Injection USP, 0.3 mg and Epinephrine Injection USP, 0.15 mg are single-dose auto-injectors and combination products containing drug and device components. Each Epinephrine Injection USP, 0.3 mg (Auto-Injector) delivers a single dose of 0.3 mg epinephrine, USP from epinephrine injection USP, 0.3 mg/0.3 mL in a sterile solution. Each Epinephrine Injection USP, 0.15 mg (Auto-Injector) delivers a single dose of 0.15 mg epinephrine, USP from epinephrine injection USP, 0.15 mg/0.3 mL in a sterile solution. Each 0.3 mL in the Epinephrine Injection USP, 0.3 mg (Auto-Injector) contains 0.3 mg epinephrine USP, 1.8 mg sodium chloride, 0.4 mg sodium metabisulfite, 0.4 mg sodium tartrate (dihydrate), hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2 to 5.0. Each 0.3 mL in the Epinephrine Injection USP, 0.15 mg (Auto-Injector) contains 0.15 mg epinephrine USP, 1.8 mg sodium chloride, 0.4 mg sodium metabisulfite, 0.2 mg sodium tartrate (dihydrate), hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2 to 5.0. Epinephrine, USP is a sympathomimetic catecholamine. Chemically, epinephrine, USP is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace Epinephrine Injection USP, 0.3 mg and Epinephrine Injection USP, 0.15 mg if the epinephrine solution appears discolored (pinkish or darker than slightly yellow), cloudy, or if it contains a precipitate. Thoroughly review the patient instructions and operation of Epinephrine Injection USP, 0.3 mg or Epinephrine Injection USP, 0.15 mg with patients and caregivers prior to use [ see Patient Counseling Information ( 17 ) ]. structure

Epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

VIATRIS SPECIALTY LLC FDA Rx Only

Epinephrine injection, USP auto-injectors, 0.3 mg and 0.15 mg, are single-dose auto-injectors and combination products containing drug and device components. Each epinephrine injection, USP auto-injector, 0.3 mg delivers a single dose of 0.3 mg epinephrine from epinephrine injection, USP 0.3 mg/0.3 mL in a sterile solution. Each epinephrine injection, USP auto-injector, 0.15 mg delivers a single dose of 0.15 mg epinephrine from epinephrine injection, USP 0.15 mg/0.3 mL in a sterile solution. Each 0.3 mL in the epinephrine injection, USP auto-injector, 0.3 mg contains 0.3 mg epinephrine, 1.8 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid to adjust pH, and Water for Injection. The pH range is 2.2-5.0. Each 0.3 mL in the epinephrine injection, USP auto-injector, 0.15 mg contains 0.15 mg epinephrine, 1.8 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid to adjust pH, and Water for Injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is (-)-3,4- Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace epinephrine injection, USP auto-injector if the epinephrine solution appears discolored (pinkish or brown color), cloudy, or contains particles. Thoroughly review the patient instructions and operation of epinephrine injection, USP auto-injector with patients and caregivers prior to use [ see Patient Counseling Information (17) ]. Epinephrine Structrual Formula

epinephrine EPINEPHRINE

EPINEPHRINE 1 mg/1 ml Injection

GLAND PHARMA LIMITED FDA Rx Only

Epinephrine Injection USP, 1 mg/mL is supplied as a sterile aqueous solution with a pH range of 2.2 to 5.0, that is colorless and nonpyrogenic. Each milliliter contains 1 mg epinephrine, sodium chloride 8.6 mg (for isotonicity), hydrochloric acid 6 mg as a dissolution agent, hydrochloric acid for pH adjustment, and water for injection, USP, q.s. Contains no preservatives or sulfites. Solution must be diluted prior to intravenous or ocular use. Epinephrine, USP is a sympathomimetic catecholamine (adrenergic agent) designated chemically as 4-[1-hydroxy-2 (methylamino) ethyl]-1,2 benzenediol, a white, microcrystalline powder. It has the following structural formula: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. epinephrine-spl-structure

Epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

A-S MEDICATION SOLUTIONS FDA Rx Only

Epinephrine Injection USP, 0.3 mg and Epinephrine Injection USP, 0.15 mg are single-dose auto-injectors and combination products containing drug and device components. Each Epinephrine Injection USP, 0.3 mg (Auto-Injector) delivers a single dose of 0.3 mg epinephrine, USP from epinephrine injection USP, 0.3 mg/0.3 mL in a sterile solution. Each Epinephrine Injection USP, 0.15 mg (Auto-Injector) delivers a single dose of 0.15 mg epinephrine, USP from epinephrine injection USP, 0.15 mg/0.3 mL in a sterile solution. Each 0.3 mL in the Epinephrine Injection USP, 0.3 mg (Auto-Injector) contains 0.3 mg epinephrine USP, 1.8 mg sodium chloride, 0.4 mg sodium metabisulfite, 0.4 mg sodium tartrate (dihydrate), hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2 to 5.0. Each 0.3 mL in the Epinephrine Injection USP, 0.15 mg (Auto-Injector) contains 0.15 mg epinephrine USP, 1.8 mg sodium chloride, 0.4 mg sodium metabisulfite, 0.2 mg sodium tartrate (dihydrate), hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2 to 5.0. Epinephrine, USP is a sympathomimetic catecholamine. Chemically, epinephrine, USP is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace Epinephrine Injection USP, 0.3 mg and Epinephrine Injection USP, 0.15 mg if the epinephrine solution appears discolored (pinkish or darker than slightly yellow), cloudy, or if it contains a precipitate. Thoroughly review the patient instructions and operation of Epinephrine Injection USP, 0.3 mg or Epinephrine Injection USP, 0.15 mg with patients and caregivers prior to use [ see Patient Counseling Information ( 17 ) ]. structure

epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

A-S MEDICATION SOLUTIONS FDA Rx Only

Epinephrine injection, USP 0.3 mg and 0.15 mg is an auto-injector and a combination product containing drug and device components. Each epinephrine injection, USP 0.3 mg delivers a single dose of 0.3 mg epinephrine from epinephrine injection, USP (0.3 mL) in a sterile solution. Each epinephrine injection, USP 0.15 mg delivers a single dose of 0.15 mg epinephrine from epinephrine injection, USP (0.15 mL) in a sterile solution. Epinephrine injection, USP 0.3 mg and epinephrine injection, USP 0.15 mg each contain 1.1 mL of epinephrine solution. 0.3 mL and 0.15 mL epinephrine solution are dispensed for epinephrine injection, USP 0.3 mg and epinephrine injection, USP 0.15 mg, respectively, when activated. The solution remaining after activation is not available for future use and should be discarded. Each 0.3 mL in epinephrine injection, USP 0.3 mg contains 0.3 mg epinephrine, 2.6 mg sodium chloride, not more than 1.5 mg chlorobutanol, 0.45 mg sodium bisulfite, hydrochloric acid and sodium hydroxide to adjust pH, and water for injection. The pH range is 2.2-5.0. Each 0.15 mL in epinephrine injection, USP 0.15 mg contains 0.15 mg epinephrine, 1.3 mg sodium chloride, not more than 0.75 mg chlorobutanol, 0.225 mg sodium bisulfite, hydrochloric acid and sodium hydroxide to adjust pH, and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace epinephrine injection, USP if the epinephrine solution appears discolored (pinkish or brown color), cloudy, or contains particles. Thoroughly review the patient instructions and operation of epinephrine injection, USP with patients and caregivers prior to use [see Patient Counseling Information ( 17 ) ]. Chemical Structure

EPINEPHRINE EPINEPHRINE

EPINEPHRINE 1 ml Injection

MEDICAL PURCHASING SOLUTIONS, LLC. FDA Rx Only

Epinephrine Injection, USP is a clear, colorless, sterile solution containing 1 mg/mL epinephrine. 1 mL Single-dose Vial: 1 mL single-dose clear glass vial containing 1 mg/mL epinephrine as a sterile, nonpyrogenic, clear and colorless solution. Each mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 8.6 mg Sodium chloride, 0.75 mg sodium metabisulfite, q.s hydrochloric acid as a dissolution and pH adjustment, and water for injection. The pH range is 2.2-5.0. 10 mL Multiple dose Vial: 10 mL multiple dose amber glass vial containing 10 mg/10 mL (1 mg/mL) epinephrine as a sterile, nonpyrogenic, clear and colorless solution. Each 1 mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 5 mg chlorobutanol as preservative, 7.5 mg sodium chloride, 0.5 mg sodium metabisulfite, q.s hydrochloric acid as a dissolution and pH adjustment, and water for injection. The pH range is 2.2-5.0. 30 mL Multiple dose Vial: 30 mL multiple dose amber glass vial containing 30 mg/30 mL epinephrine as a sterile, nonpyrogenic, clear and colorless solution. Each 1 mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 5 mg chlorobutanol as preservative, 7.5 mg sodium chloride, 0.5 mg sodium metabisulfite, q.s hydrochloric acid as a dissolution and pH adjustment, and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2- Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2- (methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. structure

Epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

SPORTPHARM, INC. DBA SPORTPHARM FDA Rx Only

Epinephrine Injection USP, 0.3 mg are single-dose auto-injectors and combination products containing drug and device components. Each Epinephrine Injection USP, 0.3 mg (Auto-Injector) delivers a single dose of 0.3 mg epinephrine, USP from epinephrine injection USP, 0.3 mg/0.3 mL in a sterile solution. Each 0.3 mL in the Epinephrine Injection USP, 0.3 mg (Auto-Injector) contains 0.3 mg epinephrine USP, 1.8 mg sodium chloride, 0.4 mg sodium metabisulfite, 0.4 mg sodium tartrate (dihydrate), hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2 to 5.0. Epinephrine, USP is a sympathomimetic catecholamine. Chemically, epinephrine, USP is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace Epinephrine Injection USP, 0.3 mg if the epinephrine solution appears discolored (pinkish or darker than slightly yellow), cloudy, or if it contains a precipitate. Thoroughly review the patient instructions and operation of Epinephrine Injection USP, 0.3 mg with patients and caregivers prior to use [ see Patient Counseling Information ( 17 ) ]. structure

epinephrine EPINEPHRINE

EPINEPHRINE 10 ml Injection

GLENMARK PHARMACEUTICALS INC., USA FDA Rx Only

Epinephrine Injection, USP is a clear, colorless, sterile solution containing 1 mg/mL epinephrine. 10 mL Multiple-Dose Vial: 10 mL multiple-dose amber glass vial containing 10 mg/10 mL (1 mg/mL) epinephrine as a sterile, nonpyrogenic, clear and colorless solution. In the 10 mL vial, each 1 mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 5.25 mg chlorobutanol hemihydrate as preservative, 7.5 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid for pH adjustment and water for injection. The pH range is 2.2 to 5.0. 30 mL Multiple Dose Vial: 30 mL multiple dose amber glass vial containing 30 mg/30 mL epinephrine as a sterile, nonpyrogenic, clear and colorless solution. In the 30 mL vial, each 1 mL of Epinephrine Injection USP solution contains 1 mg epinephrine, 5.25 mg chlorobutanol hemihydrate as preservative, 7.5 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid for pH adjustment and water for injection. The pH range is 2.2 to 5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2- (methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. structure.jpg

EPINEPHRINE EPINEPHRINE

EPINEPHRINE 1 mg/1 ml Injection

HENRY SCHEIN, INC. FDA Rx Only

Epinephrine Injection USP, 1 mg/mL is supplied as a sterile aqueous solution with a pH range of 2.2-5.0, that is colorless and nonpyrogenic. Each milliliter contains 1 mg epinephrine, sodium chloride 8.6 mg (for isotonicity), hydrochloric acid for pH adjustment, and water for injection, USP, qs. Contains no preservatives or sulfites. Solution must be diluted prior to intravenous or ocular use. Epinephrine, USP is a sympathomimetic catecholamine (adrenergic agent) designated chemically as 4-[1-hydroxy-2 (methylamino) ethyl]-1,2 benzenediol, a white, microcrystalline powder. It has the following structural formula: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Formula1.jpg

epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

AMNEAL PHARMACEUTICALS OF NEW YORK LLC FDA Rx Only

Epinephrine injection, USP 0.3 mg and 0.15 mg is an auto-injector and a combination product containing drug and device components. Each epinephrine injection, USP 0.3 mg delivers a single dose of 0.3 mg epinephrine from epinephrine injection, USP (0.3 mL) in a sterile solution. Each epinephrine injection, USP 0.15 mg delivers a single dose of 0.15 mg epinephrine from epinephrine injection, USP (0.15 mL) in a sterile solution. Epinephrine injection, USP 0.3 mg and epinephrine injection, USP 0.15 mg each contain 1.1 mL of epinephrine solution. 0.3 mL and 0.15 mL epinephrine solution are dispensed for epinephrine injection, USP 0.3 mg and epinephrine injection, USP 0.15 mg, respectively, when activated. The solution remaining after activation is not available for future use and should be discarded. Each 0.3 mL in epinephrine injection, USP 0.3 mg contains 0.3 mg epinephrine, 2.6 mg sodium chloride, not more than 1.5 mg chlorobutanol, 0.45 mg sodium bisulfite, hydrochloric acid and sodium hydroxide to adjust pH, and water for injection. The pH range is 2.2-5.0. Each 0.15 mL in epinephrine injection, USP 0.15 mg contains 0.15 mg epinephrine, 1.3 mg sodium chloride, not more than 0.75 mg chlorobutanol, 0.225 mg sodium bisulfite, hydrochloric acid and sodium hydroxide to adjust pH, and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace epinephrine injection, USP if the epinephrine solution appears discolored (pinkish or brown color), cloudy, or contains particles. Thoroughly review the patient instructions and operation of epinephrine injection, USP with patients and caregivers prior to use [see Patient Counseling Information ( 17 ) ]. Chemical Structure

Epinephrine EPINEPHRINE

EPINEPHRINE 10 ml Injection

PROPHARMA DISTRIBUTION FDA Rx Only

Epinephrine, USP is a non-selective alpha and beta-adrenergic agonist designated chemically as (R) -4-(1-Hydroxy-2-(methylamino)ethyl)benzene-1,2-diol, a white, microcrystalline powder. It has the following structural formula: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Epinephrine Injection USP, 1 mg/10 mL (0.1 mg/mL) is supplied as a sterile aqueous solution that is clear, colorless and nonpyrogenic. Each mL of the solution contains epinephrine (0.1 mg) as the active ingredient and the following inactive ingredients: citric acid monohydrate (3.3 mg), edetate disodium dihydrate (0.004 mg), sodium chloride (8.2 mg), sodium citrate dihydrate (1.5 mg), sodium metabisulfite, and Water for Injection. Hydrochloric acid solution is added to dissolve the active ingredient. Sodium hydroxide solution is added to adjust the pH. Nitrogen is used for blanketing protection. Solution must be diluted prior to intravenous use. structure

EPINEPHRINE EPINEPHRINE

EPINEPHRINE 1 ml Injection

REMEDYREPACK INC. FDA Rx Only

Epinephrine Injection, USP is a clear, colorless, sterile solution containing 1 mg/mL epinephrine. 1 mL Single-dose Vial: 1 mL single-dose clear glass vial containing 1 mg/mL epinephrine as a sterile, nonpyrogenic, clear and colorless solution. Each mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 8.6 mg Sodium chloride, 0.75 mg sodium metabisulfite, q.s hydrochloric acid as a dissolution and pH adjustment, and water for injection. The pH range is 2.2-5.0. 10 mL Multiple dose Vial: 10 mL multiple dose amber glass vial containing 10 mg/10 mL (1 mg/mL) epinephrine as a sterile, nonpyrogenic, clear and colorless solution. Each 1 mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 5 mg chlorobutanol as preservative, 7.5 mg sodium chloride, 0.5 mg sodium metabisulfite, q.s hydrochloric acid as a dissolution and pH adjustment, and water for injection. The pH range is 2.2-5.0. 30 mL Multiple dose Vial: 30 mL multiple dose amber glass vial containing 30 mg/30 mL epinephrine as a sterile, nonpyrogenic, clear and colorless solution. Each 1 mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 5 mg chlorobutanol as preservative, 7.5 mg sodium chloride, 0.5 mg sodium metabisulfite, q.s hydrochloric acid as a dissolution and pH adjustment, and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2- Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2- (methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. structure

Epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

REDPHARM DRUG FDA Rx Only

Epinephrine Injection USP, 0.3 mg and Epinephrine Injection USP, 0.15 mg are single-dose auto-injectors and combination products containing drug and device components. Each Epinephrine Injection USP, 0.3 mg (Auto-Injector) delivers a single dose of 0.3 mg epinephrine, USP from epinephrine injection USP, 0.3 mg/0.3 mL in a sterile solution. Each Epinephrine Injection USP, 0.15 mg (Auto-Injector) delivers a single dose of 0.15 mg epinephrine, USP from epinephrine injection USP, 0.15 mg/0.3 mL in a sterile solution. Each 0.3 mL in the Epinephrine Injection USP, 0.3 mg (Auto-Injector) contains 0.3 mg epinephrine USP, 1.8 mg sodium chloride, 0.4 mg sodium metabisulfite, 0.4 mg sodium tartrate (dihydrate), hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2 to 5.0. Each 0.3 mL in the Epinephrine Injection USP, 0.15 mg (Auto-Injector) contains 0.15 mg epinephrine USP, 1.8 mg sodium chloride, 0.4 mg sodium metabisulfite, 0.2 mg sodium tartrate (dihydrate), hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2 to 5.0. Epinephrine, USP is a sympathomimetic catecholamine. Chemically, epinephrine, USP is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace Epinephrine Injection USP, 0.3 mg and Epinephrine Injection USP, 0.15 mg if the epinephrine solution appears discolored (pinkish or darker than slightly yellow), cloudy, or if it contains a precipitate. Thoroughly review the patient instructions and operation of Epinephrine Injection USP, 0.3 mg or Epinephrine Injection USP, 0.15 mg with patients and caregivers prior to use [ see Patient Counseling Information ( 17 ) ]. structure

Epinephrine EPINEPHRINE

EPINEPHRINE 0.3 mg Injection

ADVANCED RX PHARMACY OF TENNESSEE, LLC FDA Rx Only

Epinephrine injection, USP 0.3 mg and 0.15 mg is an auto-injector and a combination product containing drug and device components. Each epinephrine injection, USP 0.3 mg delivers a single dose of 0.3 mg epinephrine from epinephrine injection, USP (0.3 mL) in a sterile solution. Each epinephrine injection, USP 0.15 mg delivers a single dose of 0.15 mg epinephrine from epinephrine injection, USP (0.15 mL) in a sterile solution. Epinephrine injection, USP 0.3 mg and epinephrine injection, USP 0.15 mg each contain 1.1 mL of epinephrine solution. 0.3 mL and 0.15 mL epinephrine solution are dispensed for epinephrine injection, USP 0.3 mg and epinephrine injection, USP 0.15 mg, respectively, when activated. The solution remaining after activation is not available for future use and should be discarded. Each 0.3 mL in epinephrine injection, USP 0.3 mg contains 0.3 mg epinephrine, 2.6 mg sodium chloride, not more than 1.5 mg chlorobutanol, 0.45 mg sodium bisulfite, hydrochloric acid and sodium hydroxide to adjust pH, and water for injection. The pH range is 2.2-5.0. Each 0.15 mL in epinephrine injection, USP 0.15 mg contains 0.15 mg epinephrine, 1.3 mg sodium chloride, not more than 0.75 mg chlorobutanol, 0.225 sodium bisulfite, hydrochloric acid and sodium hydroxide to adjust pH, and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace epinephrine injection, USP if the epinephrine solution appears discolored (pinkish or brown color), cloudy, or contains particles. Thoroughly review the patient instructions and operation of epinephrine injection, USP with patients and caregivers prior to use [see Patient Counseling Information (17)]. Description

EPINEPHRINE EPINEPHRINE

EPINEPHRINE 0.3 mg/0.3 ml Injection

HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

AUVI-Q (epinephrine injection, USP) 0.3 mg, 0.15 mg and 0.1 mg is an auto-injector and a combination product containing drug and device components. AUVI-Q includes audible (electronic voice instructions, beeps) and visible (LED lights) cues for use. The needle automatically retracts after the injection is complete. Each AUVI-Q 0.3 mg delivers a single dose of 0.3 mg epinephrine from epinephrine injection, USP (0.3 mL) in a sterile solution. Each AUVI-Q 0.15 mg delivers a single dose of 0.15 mg epinephrine from epinephrine injection, USP (0.15 mL) in a sterile solution. Each AUVI-Q 0.1 mg delivers a single dose of 0.1 mg epinephrine from epinephrine injection, USP (0.1 mL) in a sterile solution . AUVI-Q 0.3 mg, AUVI-Q 0.15 mg and AUVI-Q 0.1 mg each contain 0.76 mL epinephrine solution. 0.3 mL, 0.15 mL and 0.1 mL epinephrine solution is dispensed for AUVI-Q 0.3 mg, AUVI-Q 0.15 mg and AUVI-Q 0.1 mg, respectively, when activated. The remaining solution is not available for future use and should be discarded. Each 0.3 mL in AUVI-Q 0.3 mg contains 0.3 mg epinephrine, 2.3 mg sodium chloride, 0.5 mg sodium bisulfite, hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2–5.0. Each 0.15 mL in AUVI-Q 0.15 mg contains 0.15 mg epinephrine, 1.2 mg sodium chloride, 0.2 mg sodium bisulfite, hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2–5.0. Each 0.1 mL in AUVI-Q 0.1 mg contains 0.1 mg epinephrine, 0.78 mg sodium chloride, 0.15 mg sodium bisulfite, hydrochloric acid to adjust pH, and water for injection. The pH range is 2.2–5.0. Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is (-)-3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure: Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. AUVI-Q is not made with natural rubber latex. AUVI-Q instructional and safety systems should be thoroughly reviewed with patients and caregivers prior to use [see PATIENT COUNSELING INFORMATION 17 (17.1)]. STRUCTURE

EPINEPHRINE EPINEPHRINE

EPINEPHRINE 30 mg/30 ml Injection

FRESENIUS KABI USA, LLC FDA Rx Only

Epinephrine Injection, USP is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as a 30 mL solution in a multiple dose amber vial. In the 30 mL vial, each 1 mL of Epinephrine Injection, USP solution contains 1 mg epinephrine, 0.5 mg citric acid, 1 mg methylparaben (preservative), 8.6 mg sodium chloride, 0.25 mg sodium metabisulfite, hydrochloric acid for pH adjustment and water for injection. The pH range is 2.2-5.0. Solution must be diluted prior to intravenous use. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. structural formula

Adrenalinum ADRENALINUM

ADRENALINUM

OHM PHARMA INC. FDA OTC

USE: To be used according to standard homeopathic indications.

911 Adrenal Burnout and Fatigue ACETICUM AC ADRENALINUM ADRENOCORTICOTROPHIN 30X AESCULUS HIPPOCASTANUM FLOS ALFALFA ALPHA LIPOIC AC AMBRA ARG NIT AVENA SATIVA BRYONIA CARBONEUM OXYGENISATUM CARPINUS BETULUS FLOS DNA FUMARICUM ACIDUM GELSEMIUM SEMPERVIRENS HEPAR SULPHURIS CALCAREUM HYPOTHALAMUS KALI PHOSPHORICUM LACTICUM ACIDUM LECITHIN NATRUM MURIATICUM OXALICUM ACIDUM PHOSPHORICUM ACIDUM PITUITARUM POSTERIUM SARCOLACTICUM ACIDUM SELENIUM METALLICUM SEPIA SILICEA SUCCINICUM ACIDUM AND THYROIDINUM.

911 ADRENAL BURNOUT AND FATIGUE (ACETICUM AC ADR...)

KING BIO INC. FDA OTC

Uses † for temporary relief of: physical fatigue mental and emotional fatigue nervous exhaustion sluggish mind poor concentration weariness confusion apathy irritability indifference body aches lack of focus eyes sensitive to light digestive symptoms caused by stress light-headed upon standing up † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Adrenalin EPINEPHRINE

ADRENALIN (EPINEPHRINE) 1 mg/1 ml Injection

PAR HEALTH USA, LLC FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single dose clear glass vial or 30 mL of solution in a multiple dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.32 mg of 4% hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.18 mg of 4% hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Chemical Structure

Adrenalin EPINEPHRINE

ADRENALIN (EPINEPHRINE) 30 mg/30 ml Injection

PAR HEALTH USA, LLC FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 30 mL of solution in a multiple dose amber glass vial. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.18 mg of 4% hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Description

Adrenalin EPINEPHRINE

ADRENALIN (EPINEPHRINE) 1 mg/1 ml Injection

MEDICAL PURCHASING SOLUTIONS, LLC FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single dose clear glass vial or 30 mL of solution in a multiple dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Chemical Structure

Adrenalin EPINEPRINE

ADRENALIN (EPINEPRINE) 1 mg/1 ml Injection

HENRY SCHEIN, INC. FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single dose clear glass vial or 30 mL of solution in a multiple dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.32 mg of 4% hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.18 mg of 4% hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Fromula1.jpg

Adrenalin EPINEPHRINE

ADRENALIN (EPINEPHRINE) 1 mg/1 ml Injection

REMEDYREPACK INC. FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single dose clear glass vial or 30 mL of solution in a multiple dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.32 mg of 4% hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.18 mg of 4% hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Chemical Structure

Adrenalin EPINEPHRINE

ADRENALIN (EPINEPHRINE) 30 mg/30 ml Injection

PAR HEALTH USA, LLC FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 30 mL of solution in a multiple dose amber glass vial. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.18 mg of 4% hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Chemical Structure

Adrenalin EPINEPHRINE

ADRENALIN (EPINEPHRINE) 1 mg/1 ml Injection

PROPHARMA DISTRIBUTION FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single dose clear glass vial or 30 mL of solution in a multiple dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.32 mg of 4% hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.18 mg of 4% hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Chemical Structure

ADRENALIN (EPINEPHRINE) ADRENALIN EPINEPHRINE

ADRENALIN (EPINEPHRINE) (ADRENALIN EPINE...) 1 mg/ml Injection

HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

Adrenalin® (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single-use clear glass vial or 30 mL of solution in a multiple-dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin® solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin® solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. STRUCTURE

Adrenalin (epinephrine in sodium chloride) EPINEPHRINE IN SODIUM CHLORIDE

ADRENALIN (EPINEPHRINE IN SODIUM CHLORIDE) (EPINEPHRINE IN ...) 2 mg/250 ml Injection

PAR HEALTH USA, LLC FDA Rx Only

Adrenalin (epinephrine in sodium chloride injection) is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2- Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2- (methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Adrenalin (epinephrine in sodium chloride injection) is a clear, colorless, sterile solution administered by intravenous infusion, supplied in a 250 mL infusion bag. It is provided in five (5) ready-to-use concentrations containing: Ingredient Concentration 8 mcg/mL 16 mcg/mL 20 mcg/mL 32 mcg/mL 40 mcg/mL Epinephrine, USP 8 mcg 16 mcg 20 mcg 32 mcg 40 mcg Sodium chloride, USP 9 mg 9 mg 9 mg 9 mg 9 mg Disodium Edetate Dihydrate (EDTA), USP 10 mcg 10 mcg 10 mcg 10 mcg 10 mcg L (+) Tartaric Acid, NF 6.6 mcg 13.1 mcg 16.4 mcg 26.2 mcg 32.8 mcg It may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. It has a pH range of 3.7 - 4.3. The headspace in the containers has been displaced with nitrogen gas. chemical structure

ADRENALIN(R) ADRENALINR

ADRENALIN(R) (ADRENALINR) 1 mg/ml Injection

HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

Adrenalin® (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single-use clear glass vial or 30 mL of solution in a multiple-dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin® solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin® solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. STRUCTURE

Adrenalinum EPINEPHRINE

ADRENALINUM (EPINEPHRINE) 0.443 mg

BOIRON FDA OTC

Rx Only*

Adrenalinum EPINEPHRINE

ADRENALINUM (EPINEPHRINE) 0.443 mg

BOIRON FDA Rx Only

Rx Only*

Adrenalinum ADRENALINUM

ADRENALINUM

OHM PHARMA INC. FDA OTC

USE: To be used according to standard homeopathic indications.

Adrenalin Vials EPINEPHRINE

ADRENALIN VIALS (EPINEPHRINE) 1 mg/1 ml Injection

SINA HEALTH INC FDA Rx Only

Adrenalin (epinephrine injection, USP) is a clear, colorless, sterile solution containing 1 mg/mL epinephrine, packaged as 1 mL of solution in a single dose clear glass vial or 30 mL of solution in a multiple dose amber glass vial. In the 1 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 7.3 mg sodium chloride, 0.457 mg sodium metabisulfite, 1 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.32 mg of 4% hydrochloric acid to adjust pH, and water for injection. In the 30 mL vial, each 1 mL of Adrenalin solution contains 1 mg epinephrine, 6.15 mg sodium chloride, 0.457 mg sodium metabisulfite, 0.920 mg sodium hydroxide, 2.25 mg tartaric acid, 0.20 mg disodium edetate dihydrate, 5.18 mg of 4% hydrochloric acid to adjust pH, 5.25 mg chlorobutanol as a preservative and water for injection. The pH range is 2.2-5.0. Epinephrine is a sympathomimetic catecholamine. The chemical name of epinephrine is: 1,2-Benzenediol, 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-, or (-)-3,4-Dihydroxy-α-[2-(methylamino)ethyl]benzyl alcohol. The chemical structure of epinephrine is: The molecular weight of epinephrine is 183.2. Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Chemical Structure

Adrenal Liquescence GLYCYRRHIZA GLABRA ROSA CANINA ARALIA QUINQUEFOLIA GLANDULA SUPRARENALIS BOVINE ADRENALINUM CINCHONA OFFICINALIS NATRUM MURIATICUM ZINCUM METALLICUM ADRENOCORTICOTROPHIN

ADRENAL LIQUESCENCE (GLYCYRRHIZA GLA...)

NUTRITIONAL SPECIALTIES, INC. FDA OTC

USES: Provides potentized homeo-nutritional support of the adrenal.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Adrenal Liquescence GLYCYRRHIZA GLABRA ROSA CANINA ARALIA QUINQUEFOLIA AMERICAN GINSENG GLANDULA SUPRARENALIS BOVINE ADRENALINUM EPHEDRA VULGARIS NATRUM MURIATICUM ZINCUM METALLICUM ADRENOCORTICOTROPHIN

ADRENAL LIQUESCENCE (GLYCYRRHIZA GLA...)

NUTRITIONAL SPECIALTIES, INC. FDA OTC

INDICATIONS: Provides potentized homeo-nutritional support of the adrenal.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Adrenal Liquescence 3001 ADRENAL LIQUESCENCE

ADRENAL LIQUESCENCE 3001 (ADRENAL LIQUESC...)

PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS FDA OTC

INDICATIONS For the temporary relief of lethargy, lack of energy, sadness, anxiousness, or decreased ability to handle stress.*

Adrenal Support ARALIA QUINQUEFOLIA HUMULUS LUPULUS ADRENALINUM CORTISONE ACETICUM SELENIUM METALLICUM THYROIDINUM SUIS ARSENICUM ALBUM CALCAREA CARBONICA CONVALLARIA MAJALIS CROTALUS HORRIDUS FERRUM METALLICUM NUX VOMICA PHOSPHORUS SEPIA PHOSPHORICUM ACIDUM

ADRENAL SUPPORT (ARALIA QUINQUEF...)

DESERET BIOLOGICALS, INC. FDA OTC

USES: • For the temporary relief of symptoms including: • fatigue • nervous exhaustion • anxiety • forgetfulness These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Adrenal Support ARALIA QUINQUEFOLIA HUMULUS LUPULUS ADRENALINUM CORTISONE ACETICUM SELENIUM METALLICUM THYROIDINUM SUIS ARSENICUM ALBUM CALCAREA CARBONICA CONVALLARIA MAJALIS CROTALUS HORRIDUS FERRUM METALLICUM NUX VOMICA PHOSPHORUS SEPIA PHOSPHORICUM ACIDUM

ADRENAL SUPPORT (ARALIA QUINQUEF...)

DESERET BIOLOGICALS, INC. FDA OTC

USES: • For the temporary relief of symptoms including: • fatigue • nervous exhaustion • anxiety • forgetfulness These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Chlamydia Homochord Chlamydia Trachomatis CHLAMYDIA TRACHOMATIS CHLAMYDIA TRACHOMATIS WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to chlamydia infections. Male: burning sensation during urination, discharge from penis and testicular tenderness or pain. Female: vaginal discharge, burning sensation during urination, and painful sexual intercourse.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Restless Leg Symptom Relief Arsenicum album, Bufo rana, Causticum, Chamomilla, Crotalus horridus, Digitalis purpurea, Lachesis mutus, Lilium tigrinum, Pulsatilla, Rhus tox, Sulphur, Tarentula hispana, Viscum album, Zincum metallicum ARSENIC TRIOXIDE ARSENIC CATION (3+) BUFO BUFO CUTANEOUS GLAND BUFO BUFO CUTANEOUS GLAND CAUSTICUM CAUSTICUM MATRICARIA CHAMOMILLA WHOLE MATRICARIA CHAMOMILLA CROTALUS HORRIDUS HORRIDUS VENOM CROTALUS HORRIDUS HORRIDUS VENOM DIGITALIS DIGITALIS LACHESIS MUTA VENOM LACHESIS MUTA VENOM LILIUM LANCIFOLIUM WHOLE FLOWERING LILIUM LANCIFOLIUM WHOLE FLOWERING PULSATILLA VULGARIS WHOLE ANEMONE PULSATILLA TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF SULFUR SULFUR LYCOSA TARANTULA LYCOSA TARANTULA VISCUM ALBUM FRUITING TOP VISCUM ALBUM FRUITING TOP ZINC ZINC ASCORBIC ACID CITRIC ACID MONOHYDRATE CITRUS AURANTIUM FRUIT OIL ORANGE PEEL CITRUS RETICULATA FRUIT OIL WATER GLYCERIN LACTIC ACID, UNSPECIFIED FORM LONICERA JAPONICA FLOWER POLYEPSILON-LYSINE (4000 MW) CARYA OVATA BARK STEVIOL

OTC Limited

Uses For symptoms of restless legs, often worse at night: urge to move the legs heaviness muscle stiffness uneasiness in legs leg cramps burning sensation twitching, drawing, jerking legs as per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image:Restless Leg.jpg

1 Detoxification Trifolium Pratense, Capsicum Annuum, Phytolacca Decandra, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum, TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER CAPSICUM CAPSICUM PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT ALUMINUM ALUMINUM ANTIMONY TRISULFIDE ANTIMONY TRISULFIDE SILVER SILVER ARSENIC TRIOXIDE ARSENIC CATION (3+) GOLD GOLD BARIUM CARBONATE BARIUM CATION BERYLLIUM BERYLLIUM BISMUTH BISMUTH BORON BORON BROMINE BROMINE CADMIUM CADMIUM CERIUM CERIUM CESIUM CHLORIDE CESIUM CATION CHROMIUM CHROMIUM COBALT COBALT COPPER COPPER DYSPROSIUM DYSPROSIUM ERBIUM ERBIUM EUROPIUM EUROPIUM IRON IRON GADOLINIUM GADOLINIUM GERMANIUM SESQUIOXIDE GERMANIUM SESQUIOXIDE HOLMIUM HOLMIUM INDIUM INDIUM LITHIUM CARBONATE LITHIUM CATION MAGNESIUM MAGNESIUM MANGANESE MANGANESE MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS MOLYBDENUM MOLYBDENUM NEODYMIUM OXIDE NEODYMIUM OXIDE NICKEL NICKEL OSMIUM OSMIUM PALLADIUM PALLADIUM PLATINUM PLATINUM LEAD LEAD PRASEODYMIUM PRASEODYMIUM RHODIUM RHODIUM RUBIDIUM NITRITE RUBIDIUM CATION NITRITE ION SAMARIUM SAMARIUM SELENIUM SELENIUM TIN TIN STRONTIUM CARBONATE STRONTIUM CATION TERBIUM TERBIUM THALLIUM THALLIUM URANYL NITRATE HEXAHYDRATE URANIUM CATION (6+) VANADIUM VANADIUM YTTERBIUM OXIDE YTTERBIUM OXIDE ZINC ZINC BACILLUS ANTHRACIS IMMUNOSERUM RABBIT BACILLUS ANTHRACIS IMMUNOSERUM RABBIT SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND ANGUILLA ROSTRATA BLOOD SERUM ANGUILLA ROSTRATA BLOOD SERUM TARTARIC ACID TARTARIC ACID THERIDION CURASSAVICUM THERIDION CURASSAVICUM THYROID SUS SCROFA THYROID LANTHANUM LANTHANUM CORTICOTROPIN CORTICOTROPIN APIS MELLIFERA APIS MELLIFERA OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CARBO ANIMALIS CARBO ANIMALIS ACTIVATED CHARCOAL ACTIVATED CHARCOAL HUMAN BREAST TUMOR CELL HUMAN BREAST TUMOR CELL CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT STRYCHNOS WALLICHIANA BARK STRYCHNOS WALLICHIANA BARK POTASSIUM DICHROMATE DICHROMATE ION LACHESIS MUTA VENOM LACHESIS MUTA VENOM SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE PHOSPHATE ION NIOBIUM NIOBIUM PHOSPHORIC ACID PHOSPHORIC ACID PHOSPHORUS PHOSPHORUS RANCID BEEF RANCID BEEF CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM SULFURIC ACID SULFURIC ACID TANTALUM TANTALUM ALLYLTHIOUREA ALLYLTHIOUREA THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT ALCOHOL, X-RAY EXPOSED (1000 RAD) ALCOHOL, X-RAY EXPOSED (1000 RAD) CITRIC ACID MONOHYDRATE SODIUM BENZOATE ALCOHOL WATER

OTC Limited

INDICATIONS: For temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. Remedy #1 supports detoxification and cellular repair.

BioTox Hep Cochlearia Armoracia, Chelidonium Majus, Arsenicum Album, Hepar Suis, Spleen (Suis), Thymus (Suis), Hepatitis C Nosode, Hepatitis A Nosode, Hepatitis B Nosode HORSERADISH HORSERADISH CHELIDONIUM MAJUS WHOLE CHELIDONIUM MAJUS ARSENIC TRIOXIDE ARSENIC CATION (3+) PORK LIVER PORK LIVER SUS SCROFA SPLEEN SUS SCROFA SPLEEN SUS SCROFA THYMUS SUS SCROFA THYMUS HEPATITIS C VIRUS HEPATITIS C VIRUS HEPATITIS A VIRUS HEPATITIS A VIRUS HEPATITIS B VIRUS HEPATITIS B VIRUS WATER ALCOHOL

OTC Limited

INDICATIONS: Fatigue, fever, cough, flu-like symptoms, virus, pain, swelling, and stiffness of limbs.

Nexgen Restore Asclepias Vincetoxicum, Echinacea (Angustifolia), Hypothalamus (Suis), Brain (Suis), Hepar Suis, Kidney (Suis), Methylcobalamin, Pancreas Suis, Stomach (Suis), Aacg-A, Aacg-B, Calcarea Carbonica, Gambogia, Gelsemium Sempervirens, Graphites, Nux Vomica, Phytolacca Decandra, 7-Keto Dhea (Dehydroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum, Sarcolacticum Acidum, Proteus (Vulgaris) CYNANCHUM VINCETOXICUM ROOT CYNANCHUM VINCETOXICUM ROOT ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS PORK BRAIN PORK BRAIN PORK LIVER PORK LIVER PORK KIDNEY PORK KIDNEY METHYLCOBALAMIN METHYLCOBALAMIN SUS SCROFA PANCREAS SUS SCROFA PANCREAS SUS SCROFA STOMACH SUS SCROFA STOMACH APC-356433 APC-356433 APC-356434 APC-356434 OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE GAMBOGE GAMBOGE GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT GRAPHITE GRAPHITE STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT 7-KETO-DEHYDROEPIANDROSTERONE 7-KETO-DEHYDROEPIANDROSTERONE ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE GLUCAGON GLUCAGON INSULIN PORK INSULIN PORK LACTIC ACID, L- LACTIC ACID, L- PROTEUS VULGARIS PROTEUS VULGARIS WATER ALCOHOL

OTC Limited

INDICATIONS: For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, headache, fatigue, and detoxification stress.

Menopause Relief Amyl nitrosum, Calcarea carbonica, Caulophyllum thalictroides, Cimicifuga racemosa, Ferrum metallicum, Gelsemium sempervirens, Lachesis mutus, Pulsatilla, Sanguinaria canadensis, Sepia, Sulphur, Sulphuricum acidum. AMYL NITRITE AMYL NITRITE OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CAULOPHYLLUM THALICTROIDES ROOT CAULOPHYLLUM THALICTROIDES ROOT BLACK COHOSH BLACK COHOSH IRON IRON GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT LACHESIS MUTA VENOM LACHESIS MUTA VENOM PULSATILLA VULGARIS WHOLE ANEMONE PULSATILLA SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE SULFUR SULFUR SULFURIC ACID SULFURIC ACID ASCORBIC ACID CITRIC ACID MONOHYDRATE CITRUS AURANTIUM FRUIT OIL ORANGE PEEL CITRUS RETICULATA FRUIT OIL WATER GLYCERIN LACTIC ACID, UNSPECIFIED FORM LONICERA JAPONICA FLOWER POLYEPSILON-LYSINE (4000 MW) CARYA OVATA BARK STEVIOL

OTC Limited

Uses For temporary relief of of discomforts associated with menopause: hot flashes night sweats chills headaches uterine cramps mood swings sensitivity irritability fatigue poor memory As per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image: Menopause.jpg

Peptostrep Homochord Peptostreptococcus Anaerobius PEPTOSTREPTOCOCCUS ANAEROBIUS PEPTOSTREPTOCOCCUS ANAEROBIUS WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Peptostrep infection including nasal or sinus congestion, and earache.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Pyrrole 1539 Pyrrole PYRROLE PYRROLE ALCOHOL WATER

OTC Limited

INDICATIONS For the temporary relief of bloating, gas, anxiousness, insomnia, or occasional headache due to sensitivity to phenolic compounds found in foods or other products.*

Good Mood Enhancer Agrimonia eupatoria, flos, Anacardium orientale, Aurum metallicum, Avena sativa, Borago officinalis, Calcarea carbonica, Capsicum annuum, Carpinus betulus, flos, Cimicifuga racemosa, Cinchona officinalis, Hypericum perforatum, Ignatia amara, Kali bromatum, Larix decidua, flos, Natrum carbonicum, Natrum sulphuricum, Phosphoricum acidum, Phosphorus, Pulsatilla, Sepia, Sinapis arvensis, flos, Tabacum AGRIMONIA EUPATORIA FLOWER AGRIMONIA EUPATORIA FLOWER SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE GOLD GOLD AVENA SATIVA FLOWERING TOP AVENA SATIVA FLOWERING TOP BORAGE BORAGE OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CAPSICUM CAPSICUM CARPINUS BETULUS FLOWERING TOP CARPINUS BETULUS FLOWERING TOP BLACK COHOSH BLACK COHOSH CINCHONA OFFICINALIS BARK CINCHONA OFFICINALIS BARK HYPERICUM PERFORATUM WHOLE HYPERICUM PERFORATUM STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED POTASSIUM BROMIDE BROMIDE ION LARIX DECIDUA FLOWERING TOP LARIX DECIDUA FLOWERING TOP SODIUM CARBONATE CARBONATE ION SODIUM SULFATE SODIUM SULFATE ANHYDROUS PHOSPHORIC ACID PHOSPHORIC ACID PHOSPHORUS PHOSPHORUS PULSATILLA VULGARIS WHOLE ANEMONE PULSATILLA SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE SINAPIS ARVENSIS FLOWERING/FRUITING TOP SINAPIS ARVENSIS FLOWERING/FRUITING TOP TOBACCO LEAF TOBACCO LEAF ASCORBIC ACID CITRIC ACID MONOHYDRATE CITRUS AURANTIUM FRUIT OIL ORANGE PEEL CITRUS RETICULATA FRUIT OIL WATER GLYCERIN LACTIC ACID, UNSPECIFIED FORM LONICERA JAPONICA FLOWER POLYEPSILON-LYSINE (4000 MW) CARYA OVATA BARK STEVIOL

OTC Limited

Uses For temporary relief of symptoms: Melancholy Nervousness Minor mood swings Over-sensitivity Apathy Discontent Timidity Insecurity Irritability Fatigue as per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image:Good Mood.jpg

Herpes Zoster Homochord Herpes Zoster Nosode HUMAN HERPESVIRUS 3 HUMAN HERPESVIRUS 3 WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to Herpes Zoster infection including itching, tingling or painful rash usually on one side of the body or one side of the face.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Headache Relief Belladonna, Bryonia, Capsicum annuum, Chininum arsenicosum, Coffea cruda, Gelsemium sempervirens, Glonoinum, Ignatia amara, Kali bichromicum, Lycopodium clavatum, Natrum muriaticum, Nux vomica, Sanguinaria canadensis, Spigelia anthelmia, Sulphur ATROPA BELLADONNA ATROPA BELLADONNA BRYONIA ALBA ROOT BRYONIA ALBA ROOT CAPSICUM CAPSICUM QUININE ARSENITE QUININE ARABICA COFFEE BEAN ARABICA COFFEE BEAN GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT NITROGLYCERIN NITROGLYCERIN STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED POTASSIUM DICHROMATE DICHROMATE ION LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE SODIUM CHLORIDE CHLORIDE ION STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT SPIGELIA ANTHELMIA WHOLE SPIGELIA ANTHELMIA SULFUR SULFUR ASCORBIC ACID CITRIC ACID MONOHYDRATE CITRUS AURANTIUM FRUIT OIL ORANGE PEEL CITRUS RETICULATA FRUIT OIL WATER GLYCERIN LACTIC ACID, UNSPECIFIED FORM LONICERA JAPONICA FLOWER POLYEPSILON-LYSINE (4000 MW) CARYA OVATA BARK STEVIOL

OTC Limited

Uses Uses for temporary relief of various types of headache, such as: throbbing splitting tight dull sick bursting sinus congestive migraine occipital morning headache band feeling around the head sun headache as per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image:Headache Relief.jpg

Bestmade Natural Products BM224 Arnica MontD6, SangunariaD7, KalmiaD6, Rananculus BulbD10, ColchicumD7, SumbulD10, ChelidoniumD7 ALCOHOL COLCHICUM AUTUMNALE FLOWER COLCHICUM AUTUMNALE FLOWER CHELIDONIUM MAJUS WHOLE CHELIDONIUM MAJUS WHOLE SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT RANUNCULUS BULBOSUS ROOT RANUNCULUS BULBOSUS ROOT KALMIA ANGUSTIFOLIA LEAF KALMIA ANGUSTIFOLIA LEAF ARNICA MONTANA ARNICA MONTANA FERULA SUMBUL ROOT FERULA SUMBUL ROOT TASTELESS LIQUID CLEAR LIQUID

OTC Limited

It may help with shoulder pain and frozen shoulder. stiffness, and limitation in the range of movement.

Bio Holly Ilex Aquifolium (Holly), Flos ILEX AQUIFOLIUM FRUITING TOP ILEX AQUIFOLIUM FRUITING TOP WATER ALCOHOL

OTC Limited

INDICATIONS: For temporary relief of hatred, envy, jealousy, and suspicion.

Aller-Chord A Alfalfa, Allium Cepa, Ambrosia Artemisiaefolia, Bryonia (Alba), Citricum Acidum, Coumarinum, Euphrasia Officinalis, Glandula Suprarenalis Suis, Hepar Suis, Histaminum Hydrochloricum, Hydrastis Canadensis, Juniperus Communis, Mucosa Nasalis Suis, Natrum Sulphuricum, Phosphorus, Pothos Foetidus, Pulsatilla (Vulgaris), Solidago Virgaurea, Sulphur, Tanacetum Vulgare, Taraxacum Officinale, Trifolium Pratense PULSATILLA VULGARIS ANEMONE PULSATILLA SOLIDAGO VIRGAUREA FLOWERING TOP SOLIDAGO VIRGAUREA FLOWERING TOP SULFUR SULFUR TANACETUM VULGARE TOP TANACETUM VULGARE TOP TARAXACUM OFFICINALE TARAXACUM OFFICINALE TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER WATER ALCOHOL GLYCERIN ALFALFA ALFALFA ONION ONION AMBROSIA ARTEMISIIFOLIA AMBROSIA ARTEMISIIFOLIA BRYONIA ALBA ROOT BRYONIA ALBA ROOT ANHYDROUS CITRIC ACID ANHYDROUS CITRIC ACID COUMARIN COUMARIN EUPHRASIA STRICTA EUPHRASIA STRICTA SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER HISTAMINE DIHYDROCHLORIDE HISTAMINE GOLDENSEAL GOLDENSEAL JUNIPER BERRY JUNIPER BERRY SUS SCROFA NASAL MUCOSA SUS SCROFA NASAL MUCOSA SODIUM SULFATE SODIUM SULFATE ANHYDROUS PHOSPHORUS PHOSPHORUS SYMPLOCARPUS FOETIDUS ROOT SYMPLOCARPUS FOETIDUS ROOT

Aller-Chord A Alfalfa, Allium Cepa, Ambrosia Artemisiaefolia, Bryonia (Alba), Citricum Acidum, Coumarinum, Euphrasia Officinalis, Glandula Suprarenalis Suis, Hepar Suis, Histaminum Hydrochloricum, Hydrastis Canadensis, Juniperus Communis, Mucosa Nasalis Suis, Natrum Sulphuricum, Phosphorus, Pothos Foetidus, Pulsatilla (Vulgaris), Solidago Virgaurea, Sulphur, Tanacetum Vulgare, Taraxacum Officinale, Trifolium Pratense PULSATILLA VULGARIS ANEMONE PULSATILLA SOLIDAGO VIRGAUREA FLOWERING TOP SOLIDAGO VIRGAUREA FLOWERING TOP SULFUR SULFUR TANACETUM VULGARE TOP TANACETUM VULGARE TOP TARAXACUM OFFICINALE TARAXACUM OFFICINALE TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER WATER ALCOHOL GLYCERIN ALFALFA ALFALFA ONION ONION AMBROSIA ARTEMISIIFOLIA AMBROSIA ARTEMISIIFOLIA BRYONIA ALBA ROOT BRYONIA ALBA ROOT ANHYDROUS CITRIC ACID ANHYDROUS CITRIC ACID COUMARIN COUMARIN EUPHRASIA STRICTA EUPHRASIA STRICTA SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER HISTAMINE DIHYDROCHLORIDE HISTAMINE GOLDENSEAL GOLDENSEAL JUNIPER BERRY JUNIPER BERRY SUS SCROFA NASAL MUCOSA SUS SCROFA NASAL MUCOSA SODIUM SULFATE SODIUM SULFATE ANHYDROUS PHOSPHORUS PHOSPHORUS SYMPLOCARPUS FOETIDUS ROOT SYMPLOCARPUS FOETIDUS ROOT 59.1 ml

OTC Limited

Uses Temporary relief of sneezing, itching, congestion, irritated eyes.

Leaky Gut Formula Alfalfa, Fragaria Vesca, Glycyrrhiza Glabra, Aloe, Astacus Fluviatilis, Berberis Aquifolium, Lac Defloratum, Natrum Carbonicum, Saccharum Officinale, Fel Tauri, Pancreas Suis, Pepsinum, Antimonium Crudum, Carbo Vegetabilis, Euphorbium Officinarum, Lycopodium Clavatum, Magnesia Carbonica, Zincum Metallicum, Colibacillinum Cum Natrum Muriaticum, Proteus (Mirabilis) ALFALFA ALFALFA ALPINE STRAWBERRY ALPINE STRAWBERRY GLYCYRRHIZA GLABRA GLYCYRRHIZA GLABRA ALOE ALOE ASTACUS ASTACUS ASTACUS ASTACUS BERBERIS AQUIFOLIUM ROOT BARK BERBERIS AQUIFOLIUM ROOT BARK SKIM MILK SKIM MILK SODIUM CARBONATE CARBONATE ION SUCROSE SUCROSE BOS TAURUS BILE BOS TAURUS BILE SUS SCROFA PANCREAS SUS SCROFA PANCREAS PEPSIN PEPSIN ANTIMONY TRISULFIDE ANTIMONY TRISULFIDE ACTIVATED CHARCOAL ACTIVATED CHARCOAL EUPHORBIA RESINIFERA RESIN EUPHORBIA RESINIFERA RESIN LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE MAGNESIUM CARBONATE CARBONATE ION ZINC ZINC ESCHERICHIA COLI ESCHERICHIA COLI PROTEUS MIRABILIS PROTEUS MIRABILIS WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to leaky gut syndrome such as fatigue, seasonal allergies, joint pain, occasional constipation, mental fogginess and occasional diarrhea.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Bartonella Plus Arnica Montana, Echinacea (Angustifolia), Glycyrrhiza Glabra, Hydrastis Canadensis, Ledum Palustre, Thyroidinum (Suis), Arbutus Andrachne, Apis Mellifica, Arsenicum Album, Cocculus Indicus, Gunpowder, Hepar Sulphuris Calcareum, Kalmia Latifolia, Lac Caninum, Lycopodium Clavatum, Veratrum Album, Aconitum Napellus, Stramonium, Tellurium Metallicum ARNICA MONTANA ARNICA MONTANA ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA GLYCYRRHIZA GLABRA GLYCYRRHIZA GLABRA GOLDENSEAL GOLDENSEAL RHODODENDRON TOMENTOSUM LEAFY TWIG LEDUM PALUSTRE TWIG THYROID, PORCINE SUS SCROFA THYROID ARBUTUS ANDRACHNE LEAFY SHOOT ARBUTUS ANDRACHNE LEAFY SHOOT APIS MELLIFERA APIS MELLIFERA ARSENIC TRIOXIDE ARSENIC CATION (3+) ANAMIRTA COCCULUS SEED ANAMIRTA COCCULUS SEED ACTIVATED CHARCOAL ACTIVATED CHARCOAL SULFUR SULFUR POTASSIUM NITRATE NITRATE ION CALCIUM SULFIDE CALCIUM SULFIDE KALMIA LATIFOLIA LEAF KALMIA LATIFOLIA LEAF CANIS LUPUS FAMILIARIS MILK CANIS LUPUS FAMILIARIS MILK LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT ACONITUM NAPELLUS ACONITUM NAPELLUS DATURA STRAMONIUM DATURA STRAMONIUM TELLURIUM TELLURIUM WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to Bartonella such as achiness, malaise, headache, chills, backache, abdominal pain, brain fog, and neck and face discomfort.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Vax Reaction Thuja Occidentalis, Mezereum, Silicea, Calcarea Carbonica, Morbillinum, Parotidinum, Pertussinum, Poliomyelitis Nosode, Rubella Nosode, Tetanus Toxin, Carcinosin, Antimonium Crudum, Ledum Palustre, Thimerosal, Poliomyelitis Nosode THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG DAPHNE MEZEREUM BARK DAPHNE MEZEREUM BARK SILICON DIOXIDE SILICON DIOXIDE OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE MEASLES VIRUS MEASLES VIRUS MUMPS VIRUS MUMPS VIRUS BORDETELLA PERTUSSIS BORDETELLA PERTUSSIS RUBELLA VIRUS RUBELLA VIRUS CLOSTRIDIUM TETANI CLOSTRIDIUM TETANI HUMAN BREAST TUMOR CELL HUMAN BREAST TUMOR CELL ANTIMONY TRISULFIDE ANTIMONY TRISULFIDE LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG THIMEROSAL ETHYLMERCURITHIOSALICYLIC ACID POLIOVIRUS POLIOVIRUS WATER ALCOHOL

OTC Limited

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to vaccinations including fever, headache, muscle pain, rash, cough, lethargy, and aching back.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Cats Claw Uncaria Tomentosa CAT'S CLAW CAT'S CLAW WATER ALCOHOL

Cats Claw Uncaria Tomentosa CAT'S CLAW CAT'S CLAW WATER ALCOHOL 33.33 %

OTC Limited

INDICATIONS: May temporarily relieve symptoms associated with exhaustion, joint pain, and immune weakness.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Formula 2 Agnus Castus, Alpha lipoicum acidum, Androsterone 1 DHEA, Calcarea carbonica,Cinchona officinalis, Cynara Scolymus, Dopamine Hydrochloride, Hydrastis canadensis, Lycopodium clavatum, Oxytocin acetate, Quercetin, Sarcolacticum, Serotonin, Ignatia amara, Tiliroside, Ubiquinone, Valeriana Officinalis, CHASTE TREE FRUIT CHASTE TREE ALPHA LIPOIC ACID .ALPHA.-LIPOIC ACID ANDROSTERONE ANDROSTERONE OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CINCHONA OFFICINALIS BARK CINCHONA OFFICINALIS BARK CYNARA SCOLYMUS LEAF CYNARA SCOLYMUS LEAF GOLDENSEAL GOLDENSEAL LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE QUERCETIN QUERCETIN LACTIC ACID, L- LACTIC ACID, L- SEROTONIN SEROTONIN STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED TILIROSIDE TILIROSIDE UBIDECARENONE UBIDECARENONE VALERIAN VALERIAN ALCOHOL Water

OTC Limited

USES: For the temporary relief of symptoms of food cravings, including: constant appetite, increased or insatiable hunger.*

Organdrainex Allium Cepa, Allium Sativum, Ambrosia Artemisiaefolia, Berberis Vulgaris, Chelidonium Majus, Collinsonia Canadensis, Cynara Scolymus, Petroselinum Sativum, Trifolium Pratense, Methylcobalamin, Aloe, Alpha-Lipoicum Acidum, Palladium Metallicum ONION ONION GARLIC GARLIC AMBROSIA ARTEMISIIFOLIA WHOLE AMBROSIA ARTEMISIIFOLIA WHOLE BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK CHELIDONIUM MAJUS WHOLE CHELIDONIUM MAJUS WHOLE COLLINSONIA CANADENSIS ROOT COLLINSONIA CANADENSIS ROOT CYNARA SCOLYMUS LEAF CYNARA SCOLYMUS LEAF PETROSELINUM CRISPUM WHOLE PETROSELINUM CRISPUM WHOLE TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER METHYLCOBALAMIN METHYLCOBALAMIN ALOE ALOE ALPHA LIPOIC ACID ALPHA LIPOIC ACID PALLADIUM PALLADIUM ANHYDROUS CITRIC ACID POTASSIUM SORBATE WATER ALCOHOL

Organdrainex Allium Cepa, Allium Sativum, Ambrosia Artemisiaefolia, Berberis Vulgaris, Chelidonium Majus, Collinsonia Canadensis, Cynara Scolymus, Petroselinum Sativum, Trifolium Pratense, Methylcobalamin, Aloe, Alpha-Lipoicum Acidum, Palladium Metallicum ONION ONION GARLIC GARLIC AMBROSIA ARTEMISIIFOLIA WHOLE AMBROSIA ARTEMISIIFOLIA WHOLE BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK CHELIDONIUM MAJUS WHOLE CHELIDONIUM MAJUS WHOLE COLLINSONIA CANADENSIS ROOT COLLINSONIA CANADENSIS ROOT CYNARA SCOLYMUS LEAF CYNARA SCOLYMUS LEAF PETROSELINUM CRISPUM WHOLE PETROSELINUM CRISPUM WHOLE TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER METHYLCOBALAMIN METHYLCOBALAMIN ALOE ALOE ALPHA LIPOIC ACID ALPHA LIPOIC ACID PALLADIUM PALLADIUM ANHYDROUS CITRIC ACID POTASSIUM SORBATE WATER ALCOHOL 1.62 %

OTC Limited

INDICATIONS: May temporarily relieve symptoms associated with decreased lymphatic drainage of the organs, such as fatigue, headache, lymphatic swelling, and bad effects from sedentary habits.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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