Gout Symptom Relief (King Bio Inc.)


Welcome to the PulseAid listing for the Gout Symptom Relief drug offered from King Bio Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: King Bio Inc.
NON-PROPRIETARY NAME: Ammonium phosphoricum, Belladonna, Colchicum autumnale, Formicum acidum, Fraxinus excelsior, Ledum palustre, Natrum carbonicum, Nux vomica, Urtica urens
SUBSTANCE NAME: AMMONIUM PHOSPHATE, DIBASIC; ATROPA BELLADONNA; COLCHICUM AUTUMNALE BULB; FORMIC ACID; FRAXINUS EXCELSIOR BARK; FRAXINUS EXCELSIOR LEAF; LEDUM PALUSTRE TWIG; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-11-06
END MARKETING DATE: 0000-00-00


Gout Symptom Relief HUMAN OTC DRUG Details:

Item DescriptionGout Symptom Relief from King Bio Inc.
LABELER NAME: King Bio Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 10; 10; 10; 10; 10; 10; 10; 10; 10; 10([hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL)
START MARKETING DATE: 2012-11-06
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57955-0021_feebffed-535b-43dc-b78d-cb4bd5294350
PRODUCT NDC: 57955-0021
APPLICATION NUMBER:

Other AMMONIUM PHOSPHATE, DIBASIC; ATROPA BELLADONNA; COLCHICUM AUTUMNALE BULB; FORMIC ACID; FRAXINUS EXCELSIOR BARK; FRAXINUS EXCELSIOR LEAF; LEDUM PALUSTRE TWIG; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
King Bio Inc.Gout Symptom Relief
New Sun Inc.Gout Symptom Reliever
Nutra Vista Health LLC.GoutFlex Gout Symptom Formula