HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms relating to electrolyte imbalance such as dizziness and fatigue.** **These statements are based upon traditional 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
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
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.
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 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
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
4 Kids Stuffy Nose and SinusPULSATILLA PRATENSIS WHOLEOYSTER SHELL CALCIUM CARBONATE CRUDEGOLDENSEAL AND POTASSIUM DICHROMATE
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.
INDICATIONS: For temporary relief of symptoms related to heavy metal toxicity including gastritis, cough, poor concentration, nausea, vomiting, diarrhea, stomach pain, sweating, and a metallic taste in the mouth.
HGH Vitality Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-Dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, Alpha-Lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (Suis), Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis), Orchitinum (Suis), Pancreas Suis, Spleen (Suis), Human Growth Hormone CHASTE TREE CHASTE TREE AMBERGRIS AMBERGRIS CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP APIOLE (PARSLEY) APIOLE (PARSLEY) ESTRADIOL ESTRADIOL ESTRIOL ESTRIOL ESTRONE ESTRONE LEVODOPA LEVODOPA MELATONIN MELATONIN TESTOSTERONE TESTOSTERONE ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE .ALPHA.-LIPOIC ACID .ALPHA.-LIPOIC ACID NADIDE NADIDE PANTOTHENIC ACID PANTOTHENIC ACID LACTIC ACID, L- LACTIC ACID, L- UBIDECARENONE UBIDECARENONE BARIUM CARBONATE BARIUM CATION SELENIUM SELENIUM SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS SUS SCROFA LYMPH SUS SCROFA LYMPH SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW SUS SCROFA OVARY SUS SCROFA OVARY SUS SCROFA TESTICLE SUS SCROFA TESTICLE SUS SCROFA PANCREAS SUS SCROFA PANCREAS SUS SCROFA SPLEEN SUS SCROFA SPLEEN SOMATROPIN SOMATROPIN PROTEUS MORGANII PROTEUS MORGANII WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to aging including deterioration of muscles, joints and skin, sexual dysfunction, memory loss and fatigue.** **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 hypoadrenalism including fatigue, nervous exhaustion, anxiety, and forgetfulness.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Natural Fit Kali Phosphoricum, Natrum Sulphuricum, Agnus Castus, Chelidonium Majus, Fucus Vesiculosus, Lycopodium Clavatum, Thuja Occidentalis, Capsicum Annuum, Carduus Marianus, Cysteinum, Hydrocotyle Asiatica, Kali Carbonicum, Nux Vomica, Phytolacca Decandra, Rosa Canina, Flos, Salix Alba, Thea Sinensis, Gambogia, Carbo Vegetabilis, Calcarea Carbonica, Graphites, Natrum Muriaticum, Natrum Phosphoricum, Glandula Suprarenalis Suis, Hepar Suis, Pancreas Suis, Pituitarum Posterium (Bovine), Placenta Totalis Suis, DIBASIC POTASSIUM PHOSPHATE PHOSPHATE ION SODIUM SULFATE SODIUM SULFATE ANHYDROUS CHASTE TREE FRUIT CHASTE TREE FRUIT CHELIDONIUM MAJUS WHOLE CHELIDONIUM MAJUS WHOLE FUCUS VESICULOSUS FUCUS VESICULOSUS LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG CAPSICUM CAPSICUM MILK THISTLE MILK THISTLE CYSTEINE CYSTEINE CENTELLA ASIATICA WHOLE CENTELLA ASIATICA POTASSIUM CARBONATE CARBONATE ION STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT ROSA CANINA FLOWER ROSA CANINA FLOWER SALIX ALBA BARK SALIX ALBA BARK GREEN TEA LEAF GREEN TEA LEAF GAMBOGE GAMBOGE ACTIVATED CHARCOAL ACTIVATED CHARCOAL OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE GRAPHITE GRAPHITE SODIUM CHLORIDE CHLORIDE ION SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE PHOSPHATE ION SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER SUS SCROFA PANCREAS SUS SCROFA PANCREAS BOS TAURUS PITUITARY GLAND, POSTERIOR BOS TAURUS PITUITARY GLAND SUS SCROFA PLACENTA SUS SCROFA PLACENTA THYROID, BOVINE THYROID, BOVINE GYMNEMA SYLVESTRE LEAF GYMNEMA SYLVESTRE LEAF WATER WATER ALCOHOL
INDICATIONS: Spleen, Pancreas, Stomach support.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to heave metal toxicity including gastritis, cough, poor concentration, nausea, vomiting, diarrhea, stomach pain, headache, sweating, and a metallic taste in the mouth.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: To speed muscle recovery time and assist the body in replacing spent electrolytes after exertion.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Adrenal Support Aralia Quinquefolia, Humulus Lupulus, Adrenalinum, Cortisone Aceticum, Thyroidinum (Suis), Selenium Metallicum, Arsenicum Album, Calcarea Carbonica, Convallaria Majalis, Crotalus Horridus, Ferrum Metallicum, Nux Vomica, Phosphorus, Sepia, Phosphoricum Acidum AMERICAN GINSENG AMERICAN GINSENG HOPS HOPS EPINEPHRINE EPINEPHRINE CORTISONE ACETATE CORTISONE SUS SCROFA THYROID SUS SCROFA THYROID SELENIUM SELENIUM ARSENIC TRIOXIDE ARSENIC CATION (3+) OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CONVALLARIA MAJALIS CONVALLARIA MAJALIS CROTALUS HORRIDUS HORRIDUS VENOM CROTALUS HORRIDUS HORRIDUS VENOM IRON IRON STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHOSPHORUS PHOSPHORUS SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE PHOSPHORIC ACID PHOSPHORIC ACID WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to hypoadrenalism including fatigue, nervous exhaustion, anxiety, forgetfulness, and depression.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HGH Vitality Agnus Castus, Ambra Grisea, Apiolum, Estradiol, Estriol, L-Dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, alpha-Lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Conium Maculatum, Selenium Metallicum, Folliculinum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (Suis), Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis), Orchitinum (Suis), Pancreas Suis, Spleen (Suis), Human Growth Hormone, Proteus CHASTE TREE CHASTE TREE AMBERGRIS AMBERGRIS APIOLE (PARSLEY) APIOLE (PARSLEY) ESTRADIOL ESTRADIOL ESTRIOL ESTRIOL LEVODOPA LEVODOPA MELATONIN MELATONIN TESTOSTERONE TESTOSTERONE ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE .ALPHA.-LIPOIC ACID .ALPHA.-LIPOIC ACID NADIDE NADIDE PANTOTHENIC ACID PANTOTHENIC ACID LACTIC ACID, L- LACTIC ACID, L- UBIDECARENONE UBIDECARENONE BARIUM CARBONATE BARIUM CATION CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP SELENIUM SELENIUM ESTRONE ESTRONE SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS SUS SCROFA LYMPH SUS SCROFA LYMPH SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW SUS SCROFA OVARY SUS SCROFA OVARY SUS SCROFA TESTICLE SUS SCROFA TESTICLE SUS SCROFA PANCREAS SUS SCROFA PANCREAS SUS SCROFA SPLEEN SUS SCROFA SPLEEN SOMATROPIN SOMATROPIN PROTEUS MORGANII PROTEUS MORGANII LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE Convex Diamond
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to aging such as joint pain, fatigue, and foggy memory.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to the cleansing and detoxifying of the liver, such as poor digestion, irregularity and low energy levels.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms relating to electrolyte imbalance such as dizziness and fatigue.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
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.
Platinum For Women Cyanocobalamin, Glandula suprarenalis suis, Kali carbonicum, L-carnitine, L-glutamine, L-ornithine, L-tryptophan, L-tryosine, Oophorinum, CYANOCOBALAMIN CYANOCOBALAMIN SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND POTASSIUM CARBONATE POTASSIUM CATION LEVOCARNITINE LEVOCARNITINE GLUTAMINE GLUTAMINE ORNITHINE ORNITHINE TRYPTOPHAN TRYPTOPHAN TYROSINE TYROSINE SUS SCROFA OVARY SUS SCROFA OVARY SUS SCROFA THYROID SUS SCROFA THYROID OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE HUMAN CHORIONIC GONADOTROPIN HUMAN CHORIONIC GONADOTROPIN WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to aging including fatigue, minor joint pain and muscle soreness.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: Kidney, Bladder support.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.