INDICATIONS: May temporarily relieve symptoms related to mineral imbalance in the body including fatigue, dehydration, nervousness, and cramping pains.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
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
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
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
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
911 Adrenal Burnout and FatigueACETICUM AC ADRENALINUM ADRENOCORTICOTROPHIN 30X AESCULUS HIPPOCASTANUM FLOS ALFALFA ALPHA LIPOIC AC AMBRA ARG NIT AVENA SATIVA BRYONIA CARBONEUM OXYGENISATUM CARPINUS BETULUS FLOS DNA FUMARICUM ACIDUM GELSEMIUM SEMPERVIRENS HEPAR SULPHURIS CALCAREUM HYPOTHALAMUS KALI PHOSPHORICUM LACTICUM ACIDUM LECITHIN NATRUM MURIATICUM OXALICUM ACIDUM PHOSPHORICUM ACIDUM PITUITARUM POSTERIUM SARCOLACTICUM ACIDUM SELENIUM METALLICUM SEPIA SILICEA SUCCINICUM ACIDUM AND THYROIDINUM.
Uses † for temporary relief of: physical fatigue mental and emotional fatigue nervous exhaustion sluggish mind poor concentration weariness confusion apathy irritability indifference body aches lack of focus eyes sensitive to light digestive symptoms caused by stress light-headed upon standing up † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to menstrual and cyclic related conditions including emotional swings, headache, irritability, cravings and fluid retention in both menopause and andropause.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of general soreness and aching, inflammation of bones and joints, fatigue, loss of vitality, and lowered immune response.
HOMEOPATHIC INDICATIONS: For temporary relief of Rheumatoid Arthritis Symptoms such as joint pain and inflammation.** **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 general viral infection (such as influenza, Epstein-Barr virus [EBV], cytomegalovirus [CMV], hepatitis, herpes, or adenovirus) including fever, fatigue, muscle aches and pain, rash, cold sores, headache and confusion.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Ginkgo Tonic Aralia quinquefolia, Ginkgo biloba, Hydrocotyle asiatica, Polygonum multiflorum, Aronia melanocarpa, Vaccinium myrtillus, Germanium sesquioxide, Aurum metallicum Baryta muriatica, AMERICAN GINSENG AMERICAN GINSENG GINKGO GINKGO CENTELLA ASIATICA CENTELLA ASIATICA FALLOPIA MULTIFLORA ROOT FALLOPIA MULTIFLORA ROOT ARONIA MELANOCARPA FRUIT ARONIA MELANOCARPA FRUIT BILBERRY BILBERRY GERMANIUM SESQUIOXIDE GERMANIUM SESQUIOXIDE GOLD GOLD BARIUM CHLORIDE DIHYDRATE BARIUM CATION POTASSIUM PHOSPHATE, DIBASIC POTASSIUM CATION LEAD LEAD CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM TOBACCO LEAF TOBACCO LEAF VISCUM ALBUM FRUITING TOP VISCUM ALBUM FRUITING TOP UBIDECARENONE UBIDECARENONE ADENOSINE TRIPHOSPHATE ADENOSINE TRIPHOSPHATE WATER ALCOHOL
INDICATIONS: For temporary relief of coldness of the extremities; fingers and feet bluish and numb; shortness of breath on least exertion; fatigue; exhaustion and poor memory.
Veive CBD Muscle Relaxer Arnica Montana, Causticum, Rhamnus Californica, Ruta Graveolens, Taraxacum Officinale, Belladonna, Cimicifuga Racemosa, Gnaphalium Polycephalum, Hypericum Perforatum, Jatropha Curcas, Veratrum Album, Cina, Ignatia Amara, Kali Bromatum, Kali Carbonicum, Lycopodium Clavatum, Scutellaria Lateriflora, Valeriana Officinalis ARNICA MONTANA ARNICA MONTANA ALCOHOL STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED RUTA GRAVEOLENS FLOWERING TOP RUTA GRAVEOLENS FLOWERING TOP SCUTELLARIA LATERIFLORA WHOLE SCUTELLARIA LATERIFLORA WHOLE TARAXACUM OFFICINALE TARAXACUM OFFICINALE VALERIAN VALERIAN VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT ATROPA BELLADONNA ATROPA BELLADONNA CAUSTICUM CAUSTICUM ARTEMISIA CINA FLOWER ARTEMISIA CINA FLOWER CANNABIDIOL POTASSIUM SORBATE POTASSIUM BROMIDE BROMIDE ION POTASSIUM CARBONATE CARBONATE ION MEDIUM-CHAIN TRIGLYCERIDES CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) METHYL GLUCOSE DIOLEATE SODIUM HYDROXIDE GLYCERIN FRANGULA CALIFORNICA BARK FRANGULA CALIFORNICA BARK HYPERICUM PERFORATUM HYPERICUM PERFORATUM LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE WATER ANHYDROUS CITRIC ACID BLACK COHOSH BLACK COHOSH PSEUDOGNAPHALIUM OBTUSIFOLIUM PSEUDOGNAPHALIUM OBTUSIFOLIUM JATROPHA CURCAS SEED JATROPHA CURCAS SEED
Uses Uses for temporary relief of occasional: muscle cramps reslessness twitching Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
INDICATIONS: For temporary relief of symptoms related to upper respiratory infections including fever, irritated throat, swollen glands, inflamed sinus, cough and runny nose.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to poor circulation, and low energy.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HGH Vitality Agnus Castus, Ambra Grisea, Petroselinum Sativum, Estradiol, 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, GABA, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus Suis, Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis),Orchitinum (Suis),Pancreas Suis, Spleen (Suis),Hypophysis Suis, Apiolum, CHASTE TREE FRUIT CHASTE TREE AMBERGRIS AMBERGRIS PETROSELINUM CRISPUM WHOLE PETROSELINUM CRISPUM ESTRADIOL ESTRADIOL 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 .GAMMA.-AMINOBUTYRIC ACID .GAMMA.-AMINOBUTYRIC ACID 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 SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND APIOLE (PARSLEY) APIOLE (PARSLEY) PROTEUS MORGANII PROTEUS MORGANII WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to aging including fatigue, minor joint pain and muscle soreness.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, and detoxification of stress.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Lymph/Spleen Combo Juniperus Communis, Phytolacca Decandra, Quercus Glandium Spiritus, Myosotis Arvensis, Natrum Sulphuricum, Ceanothus Americanus, Helianthus Annuus, Natrum Muriaticum, Lymph (Suis), Spleen (Suis), Thymus (Suis), Chininum Arsenicosum, Castanea Vesca, Adenosinum Triphosphoricum Dinatrum, Coenzyme Q10, Ferrum Metallicum, Succinum, Apis Mellifica JUNIPERUS COMMUNIS WHOLE JUNIPERUS COMMUNIS WHOLE PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT QUERCUS ROBUR NUT QUERCUS ROBUR NUT MYOSOTIS ARVENSIS MYOSOTIS ARVENSIS SODIUM SULFATE SODIUM SULFATE ANHYDROUS CEANOTHUS AMERICANUS LEAF CEANOTHUS AMERICANUS LEAF HELIANTHUS ANNUUS FLOWERING TOP HELIANTHUS ANNUUS FLOWERING TOP SODIUM CHLORIDE CHLORIDE ION SUS SCROFA LYMPH SUS SCROFA LYMPH SUS SCROFA SPLEEN SUS SCROFA SPLEEN SUS SCROFA THYMUS SUS SCROFA THYMUS QUININE ARSENATE QUININE ARSENATE CASTANEA SATIVA LEAF CASTANEA SATIVA LEAF ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE UBIDECARENONE UBIDECARENONE IRON IRON AMBER AMBER APIS MELLIFERA APIS MELLIFERA WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to lymphatic and spleen malfunction including lack of energy, lethargy, weakness and poor muscle tone, poor appetite and sense of taste, poor digestion, loose and watery stools, poor circulation, and poor concentration.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Matrix Support Ceanothus Americanus, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (Vulgaris), Bile Duct (Suis), Colon (Suis), Duodenum (Suis), Esophagus (Suis), Eye (Suis), Gallbladder (Suis), Ileum (Suis), Intestine (Suis), Ipecacuanha, Jejunum (Suis), Kali Bichromicum, Lung, (Suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (Suis), Pancreas Suis, Phosphorus, Rectal Mucosa (Suis), Stomach (Suis CEANOTHUS AMERICANUS LEAF CEANOTHUS AMERICANUS LEAF VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE SILVER NITRATE SILVER CATION GOLDENSEAL GOLDENSEAL MOMORDICA BALSAMINA IMMATURE FRUIT MOMORDICA BALSAMINA IMMATURE FRUIT OXALIS ACETOSELLA LEAF OXALIS ACETOSELLA LEAF PULSATILLA VULGARIS ANEMONE PULSATILLA SUS SCROFA BILE DUCT SUS SCROFA BILE DUCT SUS SCROFA COLON SUS SCROFA COLON SUS SCROFA DUODENUM SUS SCROFA DUODENUM SUS SCROFA ESOPHAGUS SUS SCROFA ESOPHAGUS SUS SCROFA EYE SUS SCROFA EYE SUS SCROFA GALLBLADDER SUS SCROFA GALLBLADDER SUS SCROFA ILEUM SUS SCROFA ILEUM PORK INTESTINE PORK INTESTINE IPECAC IPECAC SUS SCROFA JEJUNUM SUS SCROFA JEJUNUM POTASSIUM DICHROMATE DICHROMATE ION SUS SCROFA LUNG SUS SCROFA LUNG SUS SCROFA NASAL MUCOSA SUS SCROFA NASAL MUCOSA SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE SUS SCROFA ORAL MUCOSA SUS SCROFA ORAL MUCOSA SUS SCROFA PANCREAS SUS SCROFA PANCREAS PHOSPHORUS PHOSPHORUS SUS SCROFA RECTAL MUCOSA SUS SCROFA RECTAL MUCOSA SUS SCROFA STOMACH SUS SCROFA STOMACH SULFUR SULFUR YEAST MANNAN YEAST MANNAN ATROPA BELLADONNA ATROPA BELLADONNA WOOD CREOSOTE WOOD CREOSOTE LACHESIS MUTA VENOM LACHESIS MUTA VENOM MANDRAGORA OFFICINARUM ROOT MANDRAGORA OFFICINARUM ROOT SUS SCROFA URINARY BLADDER SUS SCROFA URINARY BLADDER SHIGELLA DYSENTERIAE SHIGELLA DYSENTERIAE WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms such as diarrhea, constipation, headaches, gas, congestion, irritated eyes, and indigestion.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Bio Viscum Phase Viscum Album, Serotonin (Hydrochloride), Tryptophan, Adenosinum Cyclophosphoricum, Mercurius Iodatus Flavus VISCUM ALBUM FRUITING TOP VISCUM ALBUM FRUITING TOP SEROTONIN HYDROCHLORIDE SEROTONIN TRYPTOPHAN TRYPTOPHAN ADENOSINE CYCLIC PHOSPHATE ADENOSINE CYCLIC PHOSPHATE MERCUROUS IODIDE MERCUROUS IODIDE WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the termporary relief of frontal headache, rheumatism, and neuralgia.** **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 improper breakdown and excretion of allergenic substances, including gastrointestinal, skin rashes, bowel disturbance and muscle cramping.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
CORTISOL Hydrocortisone HYDROCORTISONE HYDROCORTISONE WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to adrenal glands such as joint aches, 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 Candida albicans infection such as nausea, drowsiness, lethargy, confusion, vaginal discharge, sensitivities to foods and mucous congestion.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.