Gout Symptom Reliever (New Sun Inc.)


Welcome to the PulseAid listing for the Gout Symptom Reliever drug offered from New Sun 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: New Sun 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: 2014-08-29
END MARKETING DATE: 0000-00-00


Gout Symptom Reliever HUMAN OTC DRUG Details:

Item DescriptionGout Symptom Reliever from New Sun Inc.
LABELER NAME: New Sun 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: 2014-08-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66579-0057_a0313141-41db-43b0-b885-9d78c5b5ca31
PRODUCT NDC: 66579-0057
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