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 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
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 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
By Active Ingredients
Drugs sharing any active ingredients
TOTAL FEM-BAL ADRENALINUM,PULSATILLA,CHOLESTERINUM,FOLLICULINUM,HYPOTHALAMUS,OOPHORINUM,ADRENAL CORTEX, ANDROSTENEDIONE,DHEA,PREGNANOLONE,PROGESTERONE,TESTERONE EPINEPHRINE EPINEPHRINE PULSATILLA VULGARIS PULSATILLA VULGARIS CHOLESTEROL CHOLESTEROL ESTRONE ESTRONE BOS TAURUS HYPOTHALAMUS BOS TAURUS HYPOTHALAMUS SUS SCROFA OVARY SUS SCROFA OVARY ANDROSTENEDIONE ANDROSTENEDIONE PRASTERONE PRASTERONE PREGNENOLONE PREGNENOLONE PROGESTERONE PROGESTERONE TESTOSTERONE TESTOSTERONE SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND POTASSIUM SORBATE CITRIC ACID MONOHYDRATE
INDICATIONS: For temporary relief of indigestion, flatulence, nausea, retching, vomiting after eating or drinking, minor burning in the stomach.** **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 chemical toxicity including fatigue, frequent colds, insomnia, headache, rash, occasional constipation, and memory difficulties.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Fungustat II Echinacea (angustifolia), Fucus vesiculosus, Hydrastis canadensis, Phytolacca decandra, Kreosotum, Natrum muriaticum, Candida albicans, Lycopodium clavatum, Pulsatilla (pratensis), Sepia, ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA FUCUS VESICULOSUS FUCUS VESICULOSUS GOLDENSEAL GOLDENSEAL PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT WOOD CREOSOTE WOOD CREOSOTE SODIUM CHLORIDE CHLORIDE ION CANDIDA ALBICANS CANDIDA ALBICANS LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE PULSATILLA PRATENSIS PULSATILLA PRATENSIS SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE WATER ALCOHOL
INDICATIONS: For temporary relief of bloating of the stomach, flatulence and rhinitis.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of symptoms related to petrochemical toxicity including rash, fever, pulmonary inflammation, fatigue, headache, muscle and joint pain, memory/attention disorders, frequent colds, insomnia, and depression.
Female Stimulant Aquilegia Vulgaris, Lilium Tigrinum, Bovista, Cypripedium Pubescens, Hydrastis Canadensis, Apiolum, Apis Venenum Purum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Heart (Suis), Kreosotum, Oophorinum (Suis), Uterus (Suis), Folliculinum, Aconiticum Acidum, CIS-, Lachesis Mutus, Magnesia Phosphorica, Mercurius Solubilis, Sepia, Pineal Gland (Suis), Hypophysis Suis, Estradiol, Progesterone, Testosterone, Placenta Totalis Suis, Bacillus Faecalis, Mutabile Bacillus (Bach) AQUILEGIA VULGARIS AQUILEGIA VULGARIS LILIUM LANCIFOLIUM WHOLE FLOWERING LILIUM LANCIFOLIUM WHOLE FLOWERING LYCOPERDON UTRIFORME FRUITING BODY LYCOPERDON UTRIFORME FRUITING BODY CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT GOLDENSEAL GOLDENSEAL APIOLE (PARSLEY) APIOLE (PARSLEY) APIS MELLIFERA VENOM APIS MELLIFERA VENOM SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK HEART PORK HEART WOOD CREOSOTE WOOD CREOSOTE SUS SCROFA OVARY SUS SCROFA OVARY SUS SCROFA UTERUS SUS SCROFA UTERUS ESTRONE ESTRONE ACONITIC ACID, (Z)- ACONITIC ACID, (Z)- LACHESIS MUTA VENOM LACHESIS MUTA VENOM MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE SUS SCROFA PINEAL GLAND SUS SCROFA PINEAL GLAND SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND ESTRADIOL ESTRADIOL PROGESTERONE PROGESTERONE TESTOSTERONE TESTOSTERONE SUS SCROFA PLACENTA SUS SCROFA PLACENTA ALCALIGENES FAECALIS ALCALIGENES FAECALIS ESCHERICHIA COLI ESCHERICHIA COLI WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to female hormonal problems such aas fatigue and low energy.** **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 high blood sugar including dry mouth, thirst, night sweats, sugar and carb cravings.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of the symptoms related to stress including mild anxiousness, worry, overwhelm, and mild fear.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Energize Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosus, Galium Aparine, Natrum Oxalaceticum, Thyroidinum (Suis), DHEA (Dehydroepiandrosterone), Phenyl Isothiocyanate, Tri-Iodothyronine, Tyramine, Alpha-Ketoglutaricum Acidum, Adenosinum Triphosphoricum Dinatrum, Fumaricum Acidum, Malic Acid, Colchicum Autumnale, Conium Maculatum, Funiculus Umbilicalis Suis, Hepar Suis, Medulla Ossis Suis, Pineal Gland (Suis), Spleen (Suis), Thymus (Suis), Calcarea Fluorica, Pulsatilla (Vulgaris), Spongia Tosta LACTIC ACID, L- LACTIC ACID, L- VISCUM ALBUM FRUITING TOP VISCUM ALBUM FRUITING TOP IODINE IODINE FUCUS VESICULOSUS FUCUS VESICULOSUS GALIUM APARINE GALIUM APARINE SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE THYROID, PORCINE SUS SCROFA THYROID PRASTERONE PRASTERONE PHENYL ISOTHIOCYANATE PHENYL ISOTHIOCYANATE LIOTHYRONINE LIOTHYRONINE TYRAMINE TYRAMINE ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE .ALPHA.-KETOGLUTARIC ACID .ALPHA.-KETOGLUTARIC ACID FUMARIC ACID FUMARIC ACID MALIC ACID MALIC ACID COLCHICUM AUTUMNALE BULB COLCHICUM AUTUMNALE BULB CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD PORK LIVER PORK LIVER SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW SUS SCROFA PINEAL GLAND SUS SCROFA PINEAL GLAND SUS SCROFA SPLEEN SUS SCROFA SPLEEN SUS SCROFA THYMUS SUS SCROFA THYMUS CALCIUM FLUORIDE FLUORIDE ION ANEMONE PULSATILLA ANEMONE PULSATILLA SPONGIA OFFICINALIS SKELETON, ROASTED SPONGIA OFFICINALIS SKELETON, ROASTED CORTISONE ACETATE CORTISONE MERCURIC CHLORIDE MERCURIC CATION SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS ESCHERICHIA COLI ESCHERICHIA COLI WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to the thyroid system.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Acetylcholine Chloride Phenolic Acetylcholine chloride, ACETYLCHOLINE CHLORIDE ACETYLCHOLINE WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of the symptoms of nausea and vomiting associated with pain, pregnancy, vertigo, and headache.** **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 the symptoms of fatigue.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to common bacterial infections (respiratory and urinary tract infections, food poisoning) such as fever, headache, mucous congestion, stomach discomfort, cough, joint discomfort, and diarrhea.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS FOR USE: For the temporary relief of symptoms such as: • exhaustion • dullness • drowsiness • muscle weakness Product indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms relating to headaches, fatigue and mood swings.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, headache and fatigue.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Candida Combo Candida Albicans CANDIDA ALBICANS CANDIDA ALBICANS WATER ALCOHOL
INDICATIONS: For temporary relief of gas with abdominal discomfort after eating, mood swings, joint pains, irritability, forgetfulness, skin rashes and fatigue.