sodium chloride - Medications

INDICATIONS Temporarily relieves resentment, bitterness, self-pity, hopelessness, pessimism, self-perfection, dread, or anxiousness.*

INDICATIONS Temporarily relieves anger, aggravation, irritability, overenthusiasm, hyperactivity, being overly possessive, protective, critical, manipulating, or demanding, or being easily offended.*

INDICATIONS Temporarily relieves hopelessness, sorrow, despair, mental anguish, overprotectiveness, being easily offended, irritability, anxiousness, or dread.*

INDICATIONS Temporarily relieves apathy, lost motivation, lack of ambition, inflexibility, being authoritative or bullying, self-centered, dissatisfaction, irritability, sadness, anxiousness, or anger.*

Use s For persons prone to congestion

For detail, please read the enclosed package (product information leaflet)

INDICATIONS: For temporary relief of allergies caused by poison ivy, oak, and summac.

Ringer’s Irrigation USP is a sterile, nonpyrogenic, solution of electrolytes in water for injection intended only for sterile irrigation, washing and rinsing purposes. Each 100 mL contains: Sodium Chloride USP 0.86 g; Potassium Chloride USP 0.03 g Calcium Chloride Dihydrate USP 0.033 g; Water for Injection USP qs pH: 5.8 (5.0-7.5). The solution is isotonic (310 mOsmol/liter, calc.) and has the following electrolyte content (mEq/liter): Na + 147; K + 4 Ca ++ 4.5; Cl − 156 The solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only for use as a single-dose or short procedure irrigation. When smaller volumes are required the unused portion should be discarded. Ringer’s Irrigation USP may be classified as a sterile irrigant, wash, rinse and pharmaceutical vehicle. The formulas of the active ingredients are: Ingredients Molecular Formula Molecular Weight Sodium Chloride USP NaCl 58.44 Potassium Chloride USP KCl 74.55 Calcium Chloride Dihydrate USP CaCl 2 •2H 2 O 147.01 The plastic container is a copolymer of ethylene and propylene formulated and developed for parenteral drugs. The copolymer contains no plasticizers and exhibits virtually no leachability. The plastic container is also virtually impermeable to vapor transmission and therefore, requires no overwrap to maintain the proper drug concentration. The safety of the plastic container has been confirmed by biological evaluation procedures. The material passes Class Vl testing as specified in the U.S. Pharmacopeia for Biological Tests — Plastic Containers. These tests have shown that the container is nontoxic and biologically inert. Not made with natural rubber latex, PVC or DEHP.

Ringer’s Injection USP is a sterile, nonpyrogenic solution for fluid and electrolyte replenishment in a single-dose container for intravenous administration. Composition, osmolarity, pH, ionic concentration and caloric content are shown in Table 1. Table 1 Size (mL) Composition (g/L) Osmolarity Normal physiologic osmolarity range is approximately 280 to 310 mOsmol/L. (mOsmol/L) (calc) pH Ionic Concentration (mEq/L) Caloric Content (kcal/L) Sodium Chloride, USP Calcium Chloride, USP Potassium Chloride, USP Sodium Potassium Calcium Chloride Ringer’s Injection, USP 1000 8.6 0.33 0.3 310 5.8 (5.0 to 7.5) 147 4 4.5 156 0 The chemical name, structural formula, and molecular weight of the active ingredients are shown in Table 2. Table 2 Ingredients Molecular Formula Molecular Weight Sodium Chloride USP 58.44 Potassium Chloride USP 74.55 Calcium Chloride Dihydrate USP 147.02 Not made with natural rubber latex, PVC or DEHP. The plastic container is made from a multilayered film developed for parenteral drugs. It contains no plasticizers and has minimal leachables. The solution contact layer is a rubberized copolymer of ethylene and propylene. The container-solution unit is a closed system and is not dependent upon entry of external air during administration. The container is overwrapped to provide protection from the physical environment and to provide an additional moisture barrier when necessary. The closure system has two ports; the one for the administration set has a tamper evident plastic protector and the other is a medication addition site [see Dosage and Administration (2.3) ]. Sodium Chloride USP Potassium Chloride USP Calcium Chloride Dihydrate USP

Ringer’s Irrigation, USP Each 100 mL contains: 860 mg Sodium Chloride, USP, 33 mg Calcium Chloride, USP, 30 mg Potassium Chloride, USP. No antimicrobial agent has been added. pH 6.0 (5.0 to 7.5). Osmolarity 309 mOsmol/L (calc.). Sterile, nonpyrogenic. Pour Bottle.

This product is a sterile, nonpyrogenic solutions containing isotonic concentrations of electrolytes in water for injection. The solution is isotonic. The solution is administered by intravenous infusion for parenteral replacement of extracellular losses of fluid and electrolytes, with or without minimal carbohydrate calories. Each 100 mL of Ringer's Injection, USP contains sodium chloride 860 mg, potassium chloride 30 mg and calcium chloride, dihydrate 33 mg. May contain hydrochloric acid and/or sodium hydroxide for pH adjustment. A liter provides 147 mEq sodium (Na + ), 4 mEq potassium (K + ), 4 mEq calcium (Ca ++ ) and 155 mEq chloride (Cl − ). The electrolyte content is isotonic (309 mOsmol/liter, calc.) in relation to the extracellular fluid (approx. 280 mOsmol/liter). The pH of the solution is 5.4 (5.0 − 7.5). The solution contains no bacteriostat, antimicrobial agent or added buffer (except for pH adjustment) and is intended only for use as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solution is a parenteral fluid, nutrient and/or electrolyte replenisher. Dextrose, USP is chemically designated D-glucose, monohydrate (C 6 H 12 O 6 ∙ H 2 O), a hexose sugar freely soluble in water. It has the following structural formula: Calcium Chloride, USP is chemically designated calcium chloride, dihydrate (CaCl 2 ∙ 2 H 2 O), white fragments or granules freely soluble in water. Potassium Chloride, USP is chemically designated KCl, a white granular powder freely soluble in water. Sodium Chloride, USP is chemically designated NaCI, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H 2 O. The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solution inside the plastic container also can leach out certain chemical components in very small amounts before the expiration period is attained. However, the safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. structural formula dextrose

Uses provides instant, soothing relief to dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

Uses Naturally provides instant, soothing relief dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Uses Naturally provides instant, soothing relief dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Uses Naturally provides instant, soothing relief dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Uses provides instant, soothing relief dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Uses provides instant, soothing relief dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Directions Hold the bottle upright to create a spray, Horizontally for a stream and upside down for a single drop.

This product may be used for conditions in the respiratory passages, nasal cavity or as directed by your healthcare provider.

Uses Temporarily relieves symptoms associated with General debility Fatigue Exhaustion Tension

Uses Temporarily relieves symptoms associated with: General debility Fatigue Exhaustion Tension

Uses Temporarily relieves symptoms associated with Excessive moisture Nasal discharge Watery eyes Dryness of the lips, skin, or eyes

Uses Temporarily relieves symptoms associated with: Excessive moisture Nasal discharge Watery eyes Dryness of the lips, skin or eyes.

Uses ■ Temporarily relieves symptoms of hay fever and other upper respiratory allergies, including: ■ runny nose ■ sneezing ■ itchy or watery eyes ■ itchy nose or throat ■ sinus pain ■ headache

USES: • For the temporary relief of symptoms including: • self-consciousness • shame • embarrassment • fear of strangers • lack of confidence • worthlessness •guilt • avoiding attention • hiding • excessive apologizing • fear of failure • poor eye contact These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INDICATIONS For the temporary relief of fatigue or itchy, painful, or red skin.*

Uses Indications*: May temporarily relieve signs and symptoms associated with shingles, including stinging pain, skin lesions, itching and burning associated with herpetic eruptions and infections. *As per various homeopathic materia medicas. These indications have not been evaluated by the FDA, and product has not been clinically tested.

Questions or Comments? Call 800.570.0021 Between 9am-5pm PST [email protected] siddhaflowers.com MFD by Siddha Flower Essences Oxnard, CA 93030 Made in USA Side Panel flower essences and homeopathy: Jump start your body's natural ability to heal Natural, safe and non-habit forming No contraindications. May be effectively used with drugs and other supplements Alcohol, sugar, dairy and gluten free Prepared in purified water with natural preservatives Blends time-tested natural medicine with modern technology One month supply FOUNDATIONAL REMEDIES may be used with targeted remedies stress relief daily alignment emotional detox deep-seated stress TARGETED REMEDIES sleep male balance healthy hair blood sugar female balance lung and sinus muscles and joints throat and voice youthful skin teeth and gums happy heart hearing digestion sight

Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies: -Sneezing -Runny nose -Nasal stuffiness -Post nasal drip -Removes inhaled irritants (dust, pollen) -Promotes nasal and sinus drainage -Helps reduce swelling of nasal membranes -Moisturizes dry nasal passages

Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies -Sneezing -Nasal stuffiness -Runny nose -Post nasal drip Removes inhaled irritants (dust, pollen) Removes nasal and sinus drainage Helps reduce swelling of nasal membranes Moisturizes dry nasal passages

Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies: -Sneezing -Runny nose -Nasal stuffiness -Post nasal drip -Removes inhaled irritants (dust, pollen) -Promotes nasal and sinus drainage -Helps reduce swelling of nasal membranes -Moisturizes dry nasal passages

Uses Provides moisture to soothe and hydrate dry nasal passages caused by Indoor heat, dry climate, air travel, high altitude, oxygen use, CPAP machineuse

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

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

Uses* Uses*: Homeopathic remedy for sinusitis in dogs and cats.

INDICATIONS: For temporary relief of symptoms due to chronic catarrh of sinuses.

USES: Temporarily relieves watery, runny nose, obstructed nose, post nasal drip, sinus congestion, sinus headache, and/or symptoms related to a sinus infection.**

INDICATIONS: May temporarily relieve symptoms associated with chronic sinus issues such as painful pressure and thick nasal discharge.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies -Sneezing -Nasal stuffiness -Runny nose -Post nasal drip Removes inhaled irritants (dust, pollen) Removes nasal and sinus drainage Helps reduce swelling of nasal membranes Moisturizes dry nasal passages

Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies -Sneezing -Nasal stuffiness -Runny nose -Post nasal drip Removes inhaled irritants (dust, pollen) Removes nasal and sinus drainage Helps reduce swelling of nasal membranes Moisturizes dry nasal passages

Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies -Sneezing -Nasal stuffiness -Runny nose -Post nasal drip Removes inhaled irritants (dust, pollen) Removes nasal and sinus drainage Helps reduce swelling of nasal membranes Moisturizes dry nasal passages

Indications & Usage: Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Questions or Comments? Call 800.570.0021 Between 9am-5pm PST [email protected] siddhaflowers.com MFD by Siddha Flower Essences Oxnard, CA 93030 Made in USA Side Panel homeopathy and flower essences: Jump start your body's natural ability to heal Natural, safe and non-habit forming No contraindications. May be effectively used with drugs and other supplements Alcohol, sugar, dairy and gluten free Prepared in purified water with natural preservatives Blends time-tested natural medicine with modern technology One month supply FOUNDATIONAL REMEDIES may be used with targeted remedies stress relief daily alignment emotional detox deep-seated stress TARGETED REMEDIES sleep male virility healthy hair blood sugar female balance lung and sinus muscles and joints throat and voice youthful skin teeth and gums happy heart hearing digestion sight

Each 100 mL contains: Sodium Chloride USP 0.9 g; Water for Injection USP qs pH adjusted with Hydrochloric Acid NF pH: 5.0 (4.5–7.0) Calculated Osmolarity: 310 mOsmol/liter Concentration of Electrolytes (mEq/liter): Sodium 154; Chloride 154 0.9% Sodium Chloride Irrigation USP is sterile, nonpyrogenic, isotonic and contains no bacteriostatic or antimicrobial agents. The formula of the active ingredient is: Ingredient Molecular Formula Molecular Weight Sodium Chloride USP NaCl 58.44 The plastic container is a copolymer of ethylene and propylene formulated and developed for parenteral drugs. The copolymer contains no plasticizers and exhibits virtually no leachability. The plastic container is also virtually impermeable to vapor transmission and, therefore, requires no overwrap to maintain the proper drug concentration. The safety of the plastic container has been confirmed by biological evaluation procedures. The material passes Class Vl testing as specified in the U.S. Pharmacopeia for Biological Tests — Plastic Containers. These tests have shown that the container is nontoxic and biologically inert. Not made with natural rubber latex, PVC or DEHP.

This preparation is designed solely for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. Sodium Chloride Injection USP, 0.9% is a sterile, nonpyrogenic, isotonic solution of sodium chloride and water for injection. Each mL contains sodium chloride 9 mg. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers to dilute or dissolve drugs for injection. Its chloride and sodium ion concentrations are approximately 0.154 mEq of each per milliliter and its calculated osmolality is 0.308 milliosmols per mL. The solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment, pH 5.3 (4.5 to 7.0). Sodium chloride, USP occurs as colorless cubic crystals or white crystalline powder and has a saline taste. Sodium chloride is freely soluble in water. The empirical formula for sodium chloride is NaCl, and the molecular weight is 58.44.

Sodium Chloride Injection, USP, 23.4%, is a concentrated, nonisotonic, sterile, nonpyrogenic solution of sodium chloride 234 mg in Water for Injection. pH adjusted with sodium hydroxide or hydrochloric acid if necessary. Sodium chloride is an electrolyte replenisher. It occurs as colorless cubic crystals or white crystalline powder and has a saline taste. Sodium chloride is freely soluble in water; it is soluble in glycerin and slightly soluble in alcohol. The empirical formula for sodium chloride is NaCl and the molecular weight is 58.44.

This preparation is designed solely for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. 0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride and water for injection. Each mL contains sodium chloride 9 mg. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers to dilute or dissolve drugs for injection. 0.308 mOsmol/mL (calc.). 0.9% Sodium Chloride Injection, USP contains no preservatives. The solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. pH 5.3 (4.5 to 7.0). Sodium Chloride, USP is chemically designated NaCl, a white crystalline compound freely soluble in water. The glass container is a Type I borosilicate glass and meets the requirements of the powdered glass test according to the USP standards. The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.

3% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, hypertonic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. The pH may have been adjusted with hydrochloric acid. It contains no antimicrobial agents. Composition, ionic concentration, osmolarity, and pH are shown in Table 1 . Table 1. *Normal physiological osmolarity range is approximately 280 to 310 mOsmol/L. Size (mL) Composition (g/L) Ionic Concentration (mEq/L) *Osmolarity (mOsmol/L) (calc) pH Sodium Chloride, USP (NaCl) Sodium Chloride 3% Sodium Chloride Injection, USP 500 30 513 513 1,027 5.0 (4.5 to 7.0) The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers ( free flex ® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.

0.9% Sodium Chloride Injection, USP solution is sterile and nonpyrogenic. It is a parenteral solution containing sodium chloride in water for injection intended for intravenous administration. For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1,000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solution is a parenteral fluid and electrolyte replenisher. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for injection, USP is chemically designated H 2 O. The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers ( free flex ® bag). The free flex ® + bag has a needle-free injection port and can accept standard luer lock syringes to add medication. The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.