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
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
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 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.
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.
By Active Ingredients
Drugs sharing any active ingredients
Optimal HCG Fucus vesiculosus, Cyanocobalamin, Glandula suprarenalis suis, Hepar suis, L-carnitine, Ornithine, Antimonium crudum, FUCUS VESICULOSUS FUCUS VESICULOSUS CYANOCOBALAMIN CYANOCOBALAMIN SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER LEVOCARNITINE LEVOCARNITINE ORNITHINE ORNITHINE ANTIMONY TRISULFIDE ANTIMONY HUMAN CHORIONIC GONADOTROPIN HUMAN CHORIONIC GONADOTROPIN SUS SCROFA THYROID SUS SCROFA THYROID SODIUM SULFATE SODIUM CATION OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE PANCRELIPASE PANCRELIPASE SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS GREEN TEA LEAF ILEX PARAGUARIENSIS LEAF PAULLINIA CUPANA SEED WATER ALCOHOL WITHANIA SOMNIFERA ROOT
Uses *For temporary relief of symptoms of common eye irritations: mineral accumulations, tearing, light sensitivity, eye fatigue, redness, and itching. *This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.
Emotional Eating Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (Suis), Bacopa Speciosa, Dopamine Hydrochloride, Equol, Gambogia, Oxytocin Acetate, Rhodiola, Stomach (Suis), Thyroidinum (Suis), Chininum Sulphuricum, Cina, Iodium, Lycopodium Clavatum, Phosphorus, 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 DOPAMINE HYDROCHLORIDE DOPAMINE EQUOL, (+/-)- EQUOL, (+/-)- GAMBOGE GAMBOGE OXYTOCIN ACETATE OXYTOCIN SEDUM ROSEUM ROOT SEDUM ROSEUM ROOT SUS SCROFA STOMACH SUS SCROFA STOMACH THYROID, PORCINE SUS SCROFA THYROID QUININE SULFATE QUININE ARTEMISIA CINA PRE-FLOWERING TOP ARTEMISIA CINA FLOWER IODINE IODINE LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE PHOSPHORUS PHOSPHORUS 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 homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Jet Lag and Shift Change Cocculus indicus, Colchicum autumnale, Gelsemium sempervirens, Juniperus communis, Kali carbonicum, Kali phosphoricum, Nux vomica, Passiflora incarnata, Phosphoricum acidum, Phosphorus ANAMIRTA COCCULUS SEED ANAMIRTA COCCULUS SEED COLCHICUM AUTUMNALE BULB COLCHICUM AUTUMNALE BULB GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT JUNIPER BERRY JUNIPER BERRY POTASSIUM CARBONATE CARBONATE ION POTASSIUM PHOSPHATE, DIBASIC PHOSPHATE ION STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PASSIFLORA INCARNATA FLOWERING TOP PASSIFLORA INCARNATA FLOWERING TOP PHOSPHORIC ACID PHOSPHORIC ACID PHOSPHORUS PHOSPHORUS WATER CITRIC ACID MONOHYDRATE POTASSIUM SORBATE
Uses temporarily relieves symptoms due to jet lag or shift change: fatigue, sleeplessness, irritability, nervous tension, spasmodic yawning, drowsiness.
Indication and usage Uses: temporarily relieves minor symptoms due to difficult breathing: lung and bronchial congestion wheezing hoarseness coughing attacks burning in chest bronchial mucus mucus congestion dry cough as per various homeopathic Materia Medicas Reference image lung.jpg
Gastropanpar Pancreas, Stomach, Arsenicum album, Graphites, Lycopodium clavatum, Nux vomica, Phosphorus, Syzygium jambolanum, SUS SCROFA PANCREAS SUS SCROFA PANCREAS SUS SCROFA STOMACH SUS SCROFA STOMACH ARSENIC TRIOXIDE ARSENIC CATION (3+) GRAPHITE GRAPHITE LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHOSPHORUS PHOSPHORUS SYZYGIUM CUMINI SEED SYZYGIUM CUMINI SEED WATER ALCOHOL
INDICATIONS: For temporary relief of aching of the stomach, nausea, indigestion, fullness in the abdomen, thirst, weakness, feebleness, frequent urination.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to trauma associated with a dental procedure including inflammation, swelling and pain.** **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 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.
Bio Tonsilla Phase Conium Maculatum, Dulcamara, Echinacea (Angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbicum Acidum, Coccus Cacti, Galium Aparine, CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP SOLANUM DULCAMARA TOP SOLANUM DULCAMARA TOP ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA HORSE CHESTNUT HORSE CHESTNUT ANTIMONY POTASSIUM TARTRATE ANTIMONY CATION (3+) ASCORBIC ACID ASCORBIC ACID PROTORTONIA CACTI PROTORTONIA CACTI GALIUM APARINE GALIUM APARINE GENTIANA LUTEA ROOT GENTIANA LUTEA ROOT GERANIUM ROBERTIANUM GERANIUM ROBERTIANUM PULSATILLA VULGARIS PULSATILLA VULGARIS LACTIC ACID, L- LACTIC ACID, L- ACETYLCHOLINE CHLORIDE ACETYLCHOLINE YEAST MANNAN YEAST MANNAN SUS SCROFA LYMPH SUS SCROFA LYMPH SULFUR SULFUR TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION FERRUM PHOSPHORICUM FERROSOFERRIC PHOSPHATE SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD PORK LIVER PORK LIVER SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW SUS SCROFA SPLEEN SUS SCROFA SPLEEN CORTISONE ACETATE CORTISONE SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS SUS SCROFA THYROID SUS SCROFA THYROID BARIUM CARBONATE BARIUM CATION SUS SCROFA TONSIL SUS SCROFA TONSIL WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms such as sore throat, pain, swelling, and inflammation.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to heartburn and esophageal reflux.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Uses temporarily relieves symptoms due to mental, emotional or physical stress: █ nervous tension █ body aches █ restlessness █ irritability █ oversensitivity █ sleeplessness † as per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested.
Cerebromax Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, GABA, Norepinephrine, Octopamine, Serotonin (Hydrochloride), Taurine, Adenosinum Cyclophosphoricum, Cerebrum Suis, Diencephalon (Suis), Pineal Gland (Suis), Thalamus Opticus (Suis) ACETYLCHOLINE CHLORIDE ACETYLCHOLINE EPINEPHRINE EPINEPHRINE DOPAMINE HYDROCHLORIDE DOPAMINE .GAMMA.-AMINOBUTYRIC ACID .GAMMA.-AMINOBUTYRIC ACID NOREPINEPHRINE NOREPINEPHRINE OCTOPAMINE OCTOPAMINE SEROTONIN HYDROCHLORIDE SEROTONIN TAURINE TAURINE ADENOSINE CYCLIC PHOSPHATE ADENOSINE CYCLIC PHOSPHATE SUS SCROFA CEREBRUM SUS SCROFA CEREBRUM SUS SCROFA DIENCEPHALON SUS SCROFA DIENCEPHALON SUS SCROFA PINEAL GLAND SUS SCROFA PINEAL GLAND SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms relating to sleep, memory, and emotional issues.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Mannan Phenolic Mannan YEAST MANNAN YEAST MANNAN WATER ALCOHOL
INDICATIONS: To be used according to standard homeopathic indications.** **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 attention deficit including hyperactivity and poor concentration.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Brain Balance Core Formula Acetylcholine Chloride, Dopamine, Gaba, Octopamine, Serotonin, Taurine, Adenosinum Cyclophosphoricum, Cerebrum, Diencephalon, Pineal Gland, Thalamus Opticus ACETYLCHOLINE CHLORIDE ACETYLCHOLINE DOPAMINE DOPAMINE .GAMMA.-AMINOBUTYRIC ACID .GAMMA.-AMINOBUTYRIC ACID OCTOPAMINE OCTOPAMINE SEROTONIN HYDROCHLORIDE SEROTONIN TAURINE TAURINE ADENOSINE CYCLIC PHOSPHATE ADENOSINE CYCLIC 3',5'-PHOSPHATE SUS SCROFA CEREBRUM SUS SCROFA CEREBRUM SUS SCROFA DIENCEPHALON SUS SCROFA DIENCEPHALON SUS SCROFA PINEAL GLAND SUS SCROFA PINEAL GLAND SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS WATER ALCOHOL