HUIZHOU JINSHENG MEDICAL TECHNOLOGY CO., LTD
FDA
OTC
Straighten the cleaning solution Pour it into the cleaning position for cleaning Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes,ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.
Saline Solution is intended for use in OTC ear,nose,and throat devices intended specifically to administer medicinal substances to treat ear,nose,and throat disorders.These instruments include the powder blower,dropper,ear wick,manual nebulizer pump,and nasal inhaler. If using with an OTC ear,nose,or throat device,the follow the directions provided with the device and only use as directed.
HUIZHOU JINSHENG MEDICAL TECHNOLOGY CO., LTD
FDA
OTC
Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes, ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
0.9% Sodium Chloride Injection, USP solution is sterile and nonpyrogenic. It is a parenteral solution containing sodium chloride in water for injection intended for intravenous administration. For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1,000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solution is a parenteral fluid and electrolyte replenisher. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for injection, USP is chemically designated H2O. The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (freeflex® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
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.
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
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.
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.
365 Everyday Value Be Well Cough EaseANTIMONY POTASSIUM TARTRATE BRYONIA ALBA ROOT PROTORTONIA CACTI DROSERA ROTUNDIFOLIA IPECAC PULSATILLA VULGARIS RUMEX CRISPUS ROOT PONGIA OFFICINALIS SKELETON ROASTED LOBARIA PULMONARIA
USES* temporary relieves cough due to minor throat and bronchial irritation as may occur with a cold helps relieve chest congestion due to common colds by loosening phlegm (mucus) and thinning bronchial secretions to make coughs more productive
365 Everyday Value Be Well Cough Ease for KidsANTIMONY POTASSIUM TARTRATE BRYONIA ALBA ROOT PROTORTONIA CACTI DROSERA ROTUNDIFOLIA IPECAC PULSATILLA VULGARIS RUMEX CRISPUS ROOT PONGIA OFFICINALIS SKELETON ROASTED LOBARIA PULMONARIA
Temporary relieves cough due to minor throat and bronchial irritation as may occur with a cold. Helps loosen phlegms (mucus) and thin bronchial secretions to make coughs more productive.
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.
INDICATIONS: For temporary relief of fatigue, weakness, burning skin eruptions, itching, trembling of limbs with numbness, cough with phlegm, fever, sticking pains in head and face. Vomiting, warty growths.
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.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to hormone fluctuations associated with menopause, including hot flashes, mood swings, night sweats, flushing, headache, weight gain, insomnia, weakness, and lack of energy.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: May temporarily relieve minor aches and pains of muscles and joints.** **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 heartburn and esophageal reflux.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Chronagesic Arnica Montana, Cartilago Suis, Cinnamomum, Dulcamara, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Pantothenic Acid, Placenta Totalis Suis, Rhus Tox, Sanguinaria Canadensis, Sulphur, Apiolum, Piper Nigrum, Alpha-Lipoicum Acidum, Silicea, Symphytum Officinale, Thuja Occidentalis ARNICA MONTANA ARNICA MONTANA SUS SCROFA CARTILAGE SUS SCROFA CARTILAGE CINNAMON CINNAMON SOLANUM DULCAMARA TOP SOLANUM DULCAMARA TOP SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD NADIDE NADIDE SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE PANTOTHENIC ACID PANTOTHENIC ACID SUS SCROFA PLACENTA SUS SCROFA PLACENTA TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT SULFUR SULFUR APIOLE (PARSLEY) APIOLE (PARSLEY) GREEN PEPPERCORN GREEN PEPPERCORN .ALPHA.-LIPOIC ACID .ALPHA.-LIPOIC ACID SILICON DIOXIDE SILICON DIOXIDE COMFREY ROOT COMFREY ROOT THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of mild to moderate arthritic pain and joint stiffness.** **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 hormone fluctuations associated with menopause, including hot flashes, mood swings, night sweats, flushing, headache, weakness, and lack of energy.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Bio-Immune Chelidonium Majus, Lobelia Inflata, Rumex Crispus, Sambucus Nigra, Scrophularia Nodosa, Senega Officinalis, Spongia Tosta, Taraxacum Officinale, Myristica Sebifera, Sticta Pulmonaria, Sulphur, Ustilago Maidis, Polyporus Officinalis, Candida Albicans, Carduus Marianus, Crotalus Horridus, Agaricus Muscarius, Bovista, Secale Cornutum, Anas Barbariae, Hepatis Et Cordis Extractum, Anthracinum, Arsenicum Album, Baptisia Tinctoria, Berberis Vulgaris, Botulinum, Dysentery Bacillus, Gaertner Bacillus (Bach), CHELIDONIUM MAJUS CHELIDONIUM MAJUS LOBELIA INFLATA LOBELIA INFLATA RUMEX CRISPUS ROOT RUMEX CRISPUS ROOT SAMBUCUS NIGRA FLOWERING TOP SAMBUCUS NIGRA FLOWERING TOP SCROPHULARIA NODOSA SCROPHULARIA NODOSA POLYGALA SENEGA ROOT POLYGALA SENEGA ROOT SPONGIA OFFICINALIS SKELETON, ROASTED SPONGIA OFFICINALIS SKELETON, ROASTED TARAXACUM OFFICINALE TARAXACUM OFFICINALE VIROLA SEBIFERA RESIN VIROLA SEBIFERA RESIN LOBARIA PULMONARIA LOBARIA PULMONARIA SULFUR SULFUR USTILAGO MAYDIS USTILAGO MAYDIS LARICIFOMES OFFICINALIS FRUITING BODY LARICIFOMES OFFICINALIS FRUITING BODY CANDIDA ALBICANS CANDIDA ALBICANS MILK THISTLE MILK THISTLE CROTALUS HORRIDUS HORRIDUS VENOM CROTALUS HORRIDUS HORRIDUS VENOM AMANITA MUSCARIA FRUITING BODY AMANITA MUSCARIA FRUITING BODY LYCOPERDON UTRIFORME FRUITING BODY LYCOPERDON UTRIFORME FRUITING BODY CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE BACILLUS ANTHRACIS IMMUNOSERUM RABBIT BACILLUS ANTHRACIS IMMUNOSERUM RABBIT ARSENIC TRIOXIDE ARSENIC CATION (3+) BAPTISIA TINCTORIA ROOT BAPTISIA TINCTORIA ROOT BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK CLOSTRIDIUM BOTULINUM CLOSTRIDIUM BOTULINUM SHIGELLA DYSENTERIAE SHIGELLA DYSENTERIAE SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) INFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 NIB-104 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) INFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 NIB-104 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) INFLUENZA B VIRUS B/MARYLAND/15/2016 ANTIGEN (FORMALDEHYDE INACTIVATED) INFLUENZA B VIRUS B/MARYLAND/15/2016 HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE INACTIVATED) INFLUENZA B VIRUS B/PHUKET/3073/2013 HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) VACCINIA VIRUS VACCINIA VIRUS HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED STREPTOCOCCUS PNEUMONIAE STREPTOCOCCUS PNEUMONIAE RANCID BEEF RANCID BEEF VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN WATER ALCOHOL
INDICATIONS: May temporarily relieve symptoms associated with bacterial and viral conditions, such as fever and chills, and cough.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to heartburn and esophageal reflux.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Candida Ease Borax, Thuja Occidentalis, Arsenicum Album, Kreosotum, Sulphur, Candida Parapsilosis, Candida Albicans, Aspergillus Niger, Mucor Racemosus, Candida Krusei, Candida Pseudotropicalis, Candida Tropicalis SODIUM BORATE BORATE ION THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG ARSENIC TRIOXIDE ARSENIC CATION (3+) WOOD CREOSOTE WOOD CREOSOTE SULFUR SULFUR CANDIDA PARAPSILOSIS CANDIDA PARAPSILOSIS CANDIDA ALBICANS CANDIDA ALBICANS ASPERGILLUS NIGER VAR. NIGER ASPERGILLUS NIGER VAR. NIGER MUCOR RACEMOSUS MUCOR RACEMOSUS ISSATCHENKIA ORIENTALIS WHOLE ISSATCHENKIA ORIENTALIS WHOLE KLUYVEROMYCES MARXIANUS KLUYVEROMYCES MARXIANUS CANDIDA TROPICALIS CANDIDA TROPICALIS WATER ALCOHOL
INDICATIONS: For temporary relief of acute and chronic vaginal inflammation, vaginal discharge, abdominal distention, edema in legs, extreme tiredness, indigestion with tiredness, insomnia from tiredness, vaginal itching, mental exhaustion, rheumatic nodules and stiffness, running or congested nose, swelling in the joints.
Spasm Drops AMANITA MUSCARIA FRUITING BODY, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CITRULLUS COLOCYNTHIS FRUIT PULP, COPPER, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, LEAD, SULFUR ALCOHOL WATER AMANITA MUSCARIA FRUITING BODY AMANITA MUSCARIA FRUITING BODY OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP COPPER COPPER LACHESIS MUTA VENOM LACHESIS MUTA VENOM LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION LEAD LEAD SULFUR SULFUR
Recommended for spasms, cramps, and related pain These uses are based on traditional homeopathic practice. They have not been evauated by the FDA.
Zeel SILICON DIOXIDE and COMFREY ROOT and ARNICA MONTANA ROOT and TOXICODENDRON PUBESCENS LEAF and SULFUR and SANGUINARIA CANADENSIS ROOT and SOLANUM DULCAMARA STEM and COENZYME A and NADIDE and SODIUM DIETHYL OXALACETATE and .ALPHA.-LIPOIC ACID and SUS SCROFA CARTILAGE and SUS SCROFA EMBRYO and SUS SCROFA UMBILICAL CORD and SUS SCROFA PLACENTA and SILICON DIOXIDE SILICON DIOXIDE COMFREY ROOT COMFREY ROOT ARNICA MONTANA ROOT ARNICA MONTANA ROOT TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF SULFUR SULFUR SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT SOLANUM DULCAMARA STEM SOLANUM DULCAMARA STEM COENZYME A COENZYME A NADIDE NADIDE SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE .ALPHA.-LIPOIC ACID .ALPHA.-LIPOIC ACID SUS SCROFA CARTILAGE SUS SCROFA CARTILAGE SUS SCROFA EMBRYO SUS SCROFA EMBRYO SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA PLACENTA SUS SCROFA PLACENTA CETOSTEARYL ALCOHOL ALCOHOL WATER PETROLATUM PARAFFIN
HOMEOPATHIC INDICATIONS: For temporary relief of mild to moderate arthritic pain and joint stiffness.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
To help balance and normalize appetite. Symptoms include increased or decreased appetite These uses are based on traditional homeopathic practice. They have not been evauated by the FDA.
BioE Myalgia BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA ROOT, TANACETUM VULGARE TOP, CAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, MAGNESIUM SULFATE HEPTAHYDRATE, LEAD, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, VALERIAN ALCOHOL WATER BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK BRYONIA ALBA ROOT BRYONIA ALBA ROOT TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION CAUSTICUM CAUSTICUM CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP SOLANUM DULCAMARA TOP SOLANUM DULCAMARA TOP MAGNESIUM SULFATE HEPTAHYDRATE MAGNESIUM CATION LEAD LEAD RHODODENDRON AUREUM LEAF RHODODENDRON AUREUM LEAF TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF RUTA GRAVEOLENS FLOWERING TOP RUTA GRAVEOLENS FLOWERING TOP VALERIAN VALERIAN
For pain, tenderness, weakness in muscles and joints; muscular rheumatism. These uses are based on traditional homeopathic practice. They have not been evauated by the FDA.
INDICATIONS: May temporarily relieve minor aches and pains of muscles and joints.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: May temporarily relieve minor aches and pains of muscles and joints.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Chronagesic Arnica Montana, Rhus Toxicodendron, Dulcamara, Sanguinaria Canadensis, Cartilago Suis, Coenzyme A, Funiculus Umbilicalis Suis ARNICA MONTANA ARNICA MONTANA TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF SOLANUM DULCAMARA TOP SOLANUM DULCAMARA TOP SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT SUS SCROFA CARTILAGE SUS SCROFA CARTILAGE COENZYME A COENZYME A SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD NADIDE NADIDE SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE SUS SCROFA PLACENTA SUS SCROFA PLACENTA SULFUR SULFUR CHONDROITIN SULFATE SODIUM (BOVINE) CHONDROITIN SULFATE (BOVINE) DIMETHYL SULFONE DIMETHYL SULFONE APIOLE (PARSLEY) APIOLE (PARSLEY) CINNAMIC ACID CINNAMIC ACID MENADIONE MENADIONE PIPERINE PIPERINE .ALPHA.-LIPOIC ACID .ALPHA.-LIPOIC ACID SILICON DIOXIDE COLLOIDAL SILICON DIOXIDE COMFREY ROOT COMFREY ROOT SOMATROPIN SOMATROPIN SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS ENTEROCOCCUS FAECALIS ENTEROCOCCUS FAECALIS WATER ALCOHOL