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
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.
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
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to poor concentration.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS AND USAGE For temporary relief of sour, bitter taste after eating, fullness and soreness over the liver, coated tongue, flatulence, and diarrhea alternating with constipation.
Enviro II Potassium Gluconate, Glandula Suprarenalis Suis, Hepar Suis, Canary Feathers, Standardized Cat Hair, Cattle Epithelia, Chicken Feathers, Dog Epithelia, Duck Feathers, Gerbil Epithelia, Goat Epithelia, Goose Feathers, Guinea Pig Epithelia, Hamster Epithelia, Hog Epithelia, Horse Epithelia, Mouse Epithelia, Parakeet Feathers, Rabbit Epithelia, Rat Epithelia, House, Mattress, Rug, Upholstery, Barley, Corn, Oat, Wheat, Rice, Millet, Milo, Dust Mite, Alfalfa, Golden Rod (Solidago Virguarea), Red Clover POTASSIUM GLUCONATE POTASSIUM CATION SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER SERINUS CANARIA FEATHER SERINUS CANARIA FEATHER FELIS CATUS HAIR FELIS CATUS HAIR BOS TAURUS SKIN BOS TAURUS SKIN GALLUS GALLUS FEATHER GALLUS GALLUS FEATHER CANIS LUPUS FAMILIARIS SKIN CANIS LUPUS FAMILIARIS SKIN ANAS PLATYRHYNCHOS FEATHER ANAS PLATYRHYNCHOS FEATHER MERIONES UNGUICULATUS SKIN MERIONES UNGUICULATUS SKIN CAPRA HIRCUS SKIN CAPRA HIRCUS SKIN ANSER ANSER FEATHER ANAS PLATYRHYNCHOS FEATHER CAVIA PORCELLUS SKIN CAVIA PORCELLUS SKIN MESOCRICETUS AURATUS SKIN MESOCRICETUS AURATUS SKIN SUS SCROFA SKIN SUS SCROFA SKIN EQUUS CABALLUS SKIN EQUUS CABALLUS SKIN MUS MUSCULUS SKIN MUS MUSCULUS SKIN MELOPSITTACUS UNDULATUS FEATHER MELOPSITTACUS UNDULATUS FEATHER ORYCTOLAGUS CUNICULUS SKIN ORYCTOLAGUS CUNICULUS SKIN RATTUS NORVEGICUS SKIN RATTUS NORVEGICUS SKIN HOUSE DUST HOUSE DUST BARLEY BARLEY CORN GRAIN CORN GRAIN OAT OAT WHEAT WHEAT BROWN RICE BROWN RICE MILLET MILLET SORGHUM BICOLOR WHOLE SORGHUM BICOLOR WHOLE DERMATOPHAGOIDES FARINAE DERMATOPHAGOIDES FARINAE ALFALFA ALFALFA SOLIDAGO VIRGAUREA FLOWERING TOP SOLIDAGO VIRGAUREA FLOWERING TOP TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER FAGUS GRANDIFOLIA POLLEN FAGUS GRANDIFOLIA POLLEN ULMUS AMERICANA POLLEN ULMUS AMERICANA POLLEN JUGLANS NIGRA POLLEN JUGLANS NIGRA POLLEN SALIX NIGRA POLLEN SALIX NIGRA BARK ACER NEGUNDO POLLEN ACER NEGUNDO POLLEN POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN POPULUS DELTOIDES POLLEN CARYA OVATA POLLEN CARYA OVATA POLLEN BETULA OCCIDENTALIS POLLEN BETULA OCCIDENTALIS POLLEN QUERCUS RUBRA POLLEN QUERCUS RUBRA POLLEN PLATANUS OCCIDENTALIS POLLEN PLATANUS OCCIDENTALIS POLLEN FRAXINUS AMERICANA POLLEN FRAXINUS AMERICANA POLLEN POA PRATENSIS TOP POA PRATENSIS TOP DACTYLIS GLOMERATA TOP DACTYLIS GLOMERATA TOP AGROSTIS GIGANTEA POLLEN AGROSTIS GIGANTEA POLLEN PHLEUM PRATENSE TOP PHLEUM PRATENSE TOP AMBROSIA ACANTHICARPA POLLEN AMBROSIA ACANTHICARPA POLLEN AMBROSIA TRIFIDA POLLEN AMBROSIA TRIFIDA POLLEN AMBROSIA ARTEMISIIFOLIA AMBROSIA ARTEMISIIFOLIA AMBROSIA PSILOSTACHYA POLLEN AMBROSIA PSILOSTACHYA POLLEN RUMEX ACETOSELLA POLLEN RUMEX ACETOSELLA POLLEN RUMEX CRISPUS TOP RUMEX CRISPUS TOP ARSENIC TRIOXIDE ARSENIC CATION (3+) IRIDIUM IRIDIUM PHOSPHORUS PHOSPHORUS SELENIUM SELENIUM SULFUR SULFUR HISTAMINE DIHYDROCHLORIDE HISTAMINE HYALURONIDASE HYALURONIDASE INTERFERON .GAMMA. PORCINE RECOMBINANT INTERFERON .GAMMA. PORCINE RECOMBINANT SEROTONIN HYDROCHLORIDE SEROTONIN WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to a reaction to pollens or dust including sneezing, congestion, stomach discomfort, lethargy and cough.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Appetite Control Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (Suis), Bacopa Speciosa, Equol, Gambogia, Oxytocin Acetate, Rhodiola, Stomach (Suis), Chininum Sulphuricum, Iodium, Lycopodium Clavatum, Phosphorus, Dopamine Hydrochloride, Thyroidinum (Suis), Cina, Serotonin (Hydrochloride), Morgan Gaertner ACETYL COENZYME A ACETYL COENZYME A ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE SUS SCROFA ADRENAL CORTEX SUS SCROFA ADRENAL CORTEX BACOPA MONNIERI WHOLE BACOPA MONNIERI WHOLE EQUOL, (+/-)- EQUOL, (+/-)- OXYTOCIN ACETATE OXYTOCIN SEDUM ROSEUM ROOT SEDUM ROSEUM ROOT SUS SCROFA STOMACH SUS SCROFA STOMACH QUININE SULFATE QUININE IODINE IODINE LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE PHOSPHORUS PHOSPHORUS DOPAMINE HYDROCHLORIDE DOPAMINE SUS SCROFA THYROID SUS SCROFA THYROID ARTEMISIA CINA PRE-FLOWERING TOP ARTEMISIA CINA FLOWER SEROTONIN HYDROCHLORIDE SEROTONIN SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms including constant appetite, increased or insatiable hunger.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: May temporarily relieve symptoms associated with mold allergies, such as runny nose.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms of vertigo such as faintness, vomiting, motion sickness, spinning or swaying sensation and weakness.** **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 strains, sprains, and joint pain.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils.
Iron Mix System Formula Phenylalanine, Quercetin, Rutin, Ascorbicum Acidum, Ferrum Metallicum, Ferrum Muriaticum, Ferrum Phosphoricum, Ferrum Sulphuricum, Sarcolacticum Acidum, Adrenocorticotrophin, Proteus (Vulgaris), Sycotic Co Bacillus PHENYLALANINE PHENYLALANINE QUERCETIN QUERCETIN RUTIN RUTIN ASCORBIC ACID ASCORBIC ACID IRON IRON FERRIC CHLORIDE HEXAHYDRATE FERRIC CATION FERROSOFERRIC PHOSPHATE FERROSOFERRIC PHOSPHATE FERROUS SULFATE FERROUS CATION LACTIC ACID, L- LACTIC ACID, L- CORTICOTROPIN CORTICOTROPIN PROTEUS VULGARIS PROTEUS VULGARIS ENTEROCOCCUS FAECALIS ENTEROCOCCUS FAECALIS WATER ALCOHOL
HOMEOPATHIC INDICATIONS: Temporary relief of symptoms related to Iron in foods and supplements, including fatigue, cramping and jitteriness.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Coumarin Coumarinum COUMARIN COUMARIN WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to respiratory conditions such as cough, mucous congestions. **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 rheumatism including joint pain, fever, inflammation and pain of leg(s).** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Energise RxS Sarcolacticum Acidum, Viscum Album, Iodium, Colchicum Atumnale, Conium Maculatum, Fucus Vesiculosus, Galiu Aparine, Natrum Oxalaceticum LACTIC ACID, L- LACTIC ACID, L- VISCUM ALBUM FRUITING TOP VISCUM ALBUM FRUITING TOP IODINE IODINE COLCHICUM AUTUMNALE BULB COLCHICUM AUTUMNALE BULB CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP FUCUS VESICULOSUS FUCUS VESICULOSUS GALIUM APARINE GALIUM APARINE SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE THYROID, PORCINE THYROID, PORCINE PRASTERONE PRASTERONE PHENYL ISOTHIOCYANATE PHENYL ISOTHIOCYANATE LIOTHYRONINE LIOTHYRONINE TYRAMINE TYRAMINE .ALPHA.-KETOGLUTARIC ACID .ALPHA.-KETOGLUTARIC ACID ADENOSINE TRIPHOSPHATE ADENOSINE TRIPHOSPHATE FUMARIC ACID FUMARIC ACID MALIC ACID MALIC ACID 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 PULSATILLA VULGARIS PULSATILLA VULGARIS SPONGIA OFFICINALIS SKELETON, ROASTED SPONGIA OFFICINALIS SKELETON, ROASTED CORTISONE ACETATE CORTISONE MERCURIC CHLORIDE MERCURIC CATION SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS ESCHERICHIA COLI ESCHERICHIA COLI LACTOSE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE Convex diamond;outline
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms including slight fever, headache, chills, backache, and malaise.** **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 rheumatism including joint pain, fever, inflammation and pain of leg(s).** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.