USES: • For the temporary relief of symptoms including: • terror • horror • stress • fight or flight • nightmares • difficulty sleeping • easy irritability • difficulty concentrating • restlessness These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
PTS/Stress RemedyACONITUM NAPELLUS AMBRA GRISEA ARGEMONE MEXICANA ARNICA MONTANA ARSENICUM ALBUM BUTHUS AUSTRALIS CACAO CALCAREA CARBONICA CEREBRUM SUIS CICUTA VIROSA GLANDULA SUPRARENALIS SUIS HYOSCYAMUS NIGER IGNATIA AMARA KALI PHOSPHORICUM LILIUM TIGRINUM LITHIUM CARBONICUM NATRUM MURIATICUM PHOSPHORICUM ACIDUM STRAMONIUM TARENTULA HISPANA
USES: • For the temporary relief of symptoms including: • terror • horror • stress • fight or flight • nightmares • difficulty sleeping • easy irritability • difficulty concentrating • restlessness These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HUIZHOU JINSHENG MEDICAL TECHNOLOGY CO., LTD
FDA
OTC
Straighten the cleaning solution Pour it into the cleaning position for cleaning Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes,ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.
Saline Solution is intended for use in OTC ear,nose,and throat devices intended specifically to administer medicinal substances to treat ear,nose,and throat disorders.These instruments include the powder blower,dropper,ear wick,manual nebulizer pump,and nasal inhaler. If using with an OTC ear,nose,or throat device,the follow the directions provided with the device and only use as directed.
HUIZHOU JINSHENG MEDICAL TECHNOLOGY CO., LTD
FDA
OTC
Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes, ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. It contains no antimicrobial agents. The pH ranges from 4.5 to 7.0. Composition, osmolarity, and ionic concentration are shown below: 0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride, USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L sodium and 154 mEq/L chloride. The FLEBOFLEX and FLEBOFLEX LUER plastic containers are fabricated from latex-free polyolefins or polypropylene plastic materials. The solution contact materials do not contain PVC, DEHP, or other plasticizers. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. The suitability of the container materials has been established through biological evaluations, which have shown the containers pass Class VI U.S. Pharmacopeia (USP) testing for plastic containers. These tests confirm the biological safety of the container systems.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
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 H2O. The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (freeflex® 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.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations 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 solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. 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. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations 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 solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. 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. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
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.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations 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 solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. 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. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.
12 CELL SALTS COMPLEXCALCAREA FLUORICA CALCAREA PHOSPHORICA CALCAREA SULPHURICA FERRUM PHOSPHORICUM KALI MURIATICUM KALI PHOSPHORICUM KALI SULPHURICUM MAGNESIA PHOSPHORICA NATRUM MURIATICUM NATRUM PHOSPHORICUM NATRUM SULPHURICUM SILICEA
INDICATIONS: For weight management and inflammation support. This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
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.
4 Kids Cold and Cough DaytimeONION CALCIUM SULFIDE SODIUM CHLORIDE PHOSPHORUS PULSATILLA VULGARIS SULFUR AND GOLDENSEAL
Uses* ■ Helps temporarily relieve symptoms of common cold in children at night, including: ■ cough ■ runny nose ■ post nasal drip ■ sneezing ■ sore throat ■ nasal or chest congestion ■ occasional sleeplessness
Uses ■ Helps temporarily relieve symptoms of common cold in children at night, including: ■ cough ■ runny nose ■ post nasal drip ■ sneezing ■ sore throat ■ nasal or chest congestion ■ occasional sleeplessness
4 Kids Cold and Mucus NighttimeEUPHRASIA STRICTASILICON DIOXIDE RUMEX CRISPUS ROOT ANEMONE PULSATILLA GOLDENSEAL SODIUM CHLORIDE PHOSPHORUS ONION BRYONIA ALBA ROOT MATRICARIA CHAMOMILLA ARABICA COFFEE BEAN CALCIUM SULFIDE AND SULFUR
Uses Temporarily relieves the symptoms of the common cold in children especially at night including accumulation of mucus in chest, throat and nose, cough with mucus, runny nose, sneezing, nasal congestion and occasional sleeplessness.
4 KIDS COLD N COUGH GRAPE FLAVORONION CALCIUM SULFIDE GOLDENSEAL SODIUM CHLORIDE PHOSPHORUS ANEMONE PULSATILLA AND SULFUR
Uses ■Temporarily relieves symptoms of common cold in children, including: ■ accumulation of mucus in chest, throat or nose ■ cough with expectoration of thick, discolored mucus ■ runny nose ■ sneezing ■ nasal or chest congestion
By Active Ingredients
Drugs sharing any active ingredients
Thyropath Homeopathic Liquid AVENA SATIVA FLOWERING TOP AVENA SATIVA FLOWERING TOP BORAGE BORAGE OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CHELIDONIUM MAJUS CHELIDONIUM MAJUS FERROUS IODIDE FERROUS IODIDE FUCUS VESICULOSUS FUCUS VESICULOSUS SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER IODINE IODINE POTASSIUM IODIDE IODIDE ION PHOSPHORIC ACID PHOSPHORIC ACID SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND PYRIDOXINE HYDROCHLORIDE PYRIDOXINE THYROID, UNSPECIFIED THYROID, UNSPECIFIED ZINC ZINC WATER GLYCERIN ALCOHOL
INDICATIONS For the temporary relief of slow or difficult comprehension, milk intolerance, relief of minor feeling of forgetfulness, lack of assertiveness, shyness and apprehension associated with academically challenged children
HCG with Slimming Herbs Fucus vesiculosus, Cyanocobalamin, Glandula suprarenalis suis, Hepar suis, L-carnitine, Ornithine, Antimonium crudum, Human chorionic gonadotropin, FUCUS VESICULOSUS FUCUS VESICULOSUS CYANOCOBALAMIN CYANOCOBALAMIN SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER Levocarnitine Levocarnitine ORNITHINE ORNITHINE ANTIMONY TRISULFIDE ANTIMONY HUMAN CHORIONIC GONADOTROPIN HUMAN CHORIONIC GONADOTROPIN SUS SCROFA THYROID SUS SCROFA THYROID SODIUM SULFATE SODIUM CATION OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE PANCRELIPASE PANCRELIPASE SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS GREEN TEA LEAF ILEX PARAGUARIENSIS LEAF PAULLINIA CUPANA SEED WATER ALCOHOL WITHANIA SOMNIFERA ROOT HYDROXYCITRIC ACID
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Herpes Zoster infection including itching, tingling, burning, or painful rash usually on one side of the body or one side of the face, liver pain and mouth ulcers.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the relief of symptoms related to sensitivity to milk or milk products including skin rash, hives, vomiting, bloating, cramping and diarrhea.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Jet Lag, general body aches, nervousness, muscle cramps, sleep dysfunction, and fatigue.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of symptoms related to L-Dopa sensitivity including obesity, osteoporosis, hypertension, diabetes mellitus, arrhythmia and depression.
INDICATIONS: For temporary relief of pain in the abdomen extending around to the back, pain in the thighs and loins on urinating and frequent urination.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Lyme Disease or other viruses including joint pain, severe headache, fever, severe muscle aches/pain, flu-like feelings of headache, stiff neck, fever, muscle aches, and profound fatigue, circular rash surrounding the site of a tick bite, and change in smell/taste, difficulty chewing, swallowing, or speaking; hoarseness or vocal cord problems.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS Provides homeopathic aid for the temporary relief of symptoms related to sleep dysfunction, depression, nervous anxiety, weakness and lethargy.
INDICATIONS: For temporary relief of symptoms related to Gaba sensitivity including hypertension, anger, hostility, Seasonal Affective Disorder, sleep difficulties, fatigue, depression, food sensitivities and sleep disorders.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Lymph Plus Geranium robertianum, Nasturtium aquaticum, Aloe socotrina, Juglans regia, Myosotis, arvensis, Scrophularia nodosa, Teucrium scordonia, Apis mellifica, Equisetum hyemale, Fumaria officinalis, Natrum sulphuricum, Phytolacca decandra, Pinus sylvestris, Veronica officinalis, GERANIUM ROBERTIANUM GERANIUM ROBERTIANUM RORIPPA NASTURTIUM-AQUATICUM RORIPPA NASTURTIUM-AQUATICUM ALOE ALOE JUGLANS REGIA FLOWERING TOP JUGLANS REGIA FLOWERING TOP MYOSOTIS ARVENSIS MYOSOTIS ARVENSIS SCROPHULARIA NODOSA SCROPHULARIA NODOSA TEUCRIUM SCORODONIA FLOWERING TOP TEUCRIUM SCORODONIA FLOWERING TOP APIS MELLIFERA APIS MELLIFERA EQUISETUM HYEMALE EQUISETUM HYEMALE FUMARIA OFFICINALIS FLOWERING TOP FUMARIA OFFICINALIS FLOWERING TOP SODIUM SULFATE SODIUM CATION PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT PINUS SYLVESTRIS FLOWERING TOP PINUS SYLVESTRIS FLOWERING TOP VERONICA OFFICINALIS FLOWERING TOP VERONICA OFFICINALIS FLOWERING TOP GENTIANA LUTEA ROOT GENTIANA LUTEA ROOT SMILAX REGELII ROOT SMILAX REGELII ROOT BARIUM CARBONATE BARIUM CATION CALCIUM SULFIDE CALCIUM CATION SUS SCROFA PARATHYROID GLAND SUS SCROFA PARATHYROID GLAND SUS SCROFA THYMUS SUS SCROFA THYMUS THYROID, PORCINE THYROID, PORCINE WATER ALCOHOL
INDICATIONS: Temporary relief of symptoms related to improper levels of stomach acid, including heartburn, dyspepsia and bowel irregularity.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Pneumopar Lobelia Inflata, Symphytum Officinale, Lung (Suis), Arsenicum Album, Blatta Orientalis, Bryonia (Alba), Phosphorus, Silicea, Sulphur LOBELIA INFLATA LOBELIA INFLATA COMFREY ROOT COMFREY ROOT SUS SCROFA LUNG SUS SCROFA LUNG ARSENIC TRIOXIDE ARSENIC CATION (3+) BLATTA ORIENTALIS BLATTA ORIENTALIS BRYONIA ALBA ROOT BRYONIA ALBA ROOT PHOSPHORUS PHOSPHORUS SILICON DIOXIDE SILICON DIOXIDE SULFUR SULFUR WATER ALCOHOL
INDICATIONS: For temporary relief of wheezing, shortness of breath, bronchial spasms and cough.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HGH Plus IGF1 and IGF2 Arnica Montana, Deer Antler Velvet, Hepar Bovine, HGH, IGF, Pituitaria Glandula Bovine, Thuja Occidentalis ARNICA MONTANA ARNICA MONTANA CERVUS ELAPHUS VELVET CERVUS ELAPHUS VELVET BEEF LIVER BEEF LIVER SOMATROPIN SOMATROPIN MECASERMIN MECASERMIN BOS TAURUS PITUITARY GLAND BOS TAURUS PITUITARY GLAND THUJA OCCIDENTALIS LEAF THUJA OCCIDENTALIS LEAF WATER ALCOHOL
INDICATIONS: Temporarily supports the body to rebalance Human Growth Hormone (HGH) output. Symptoms of imbalanced HGH may include: poor muscle/fat balance, dry wrinkled-looking skin, low energy, sleeplessness, weak immune system.