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 Description | Gout Symptom Reliever from New Sun Inc. |
LABELER NAME: | New Sun Inc. |
DEA SCHEDULE: |
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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: