Menthol and Zinc Oxide (Dynarex Corporation)
Welcome to the PulseAid listing for the Menthol and Zinc Oxide drug offered from Dynarex Corporation. 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: | Dynarex Corporation |
NON-PROPRIETARY NAME: | Menthol and Zinc Oxide |
SUBSTANCE NAME: | MENTHOL; ZINC OXIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | OINTMENT |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2010-05-11 |
END MARKETING DATE: | 0000-00-00 |
Menthol and Zinc Oxide HUMAN OTC DRUG Details:
Item Description | Menthol and Zinc Oxide from Dynarex Corporation |
LABELER NAME: | Dynarex Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | .44; 21(g/100g; g/100g) |
START MARKETING DATE: | 2010-05-11 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 67777-234_5c83272b-4e2b-4400-b709-681fdc60b895 |
PRODUCT NDC: | 67777-234 |
APPLICATION NUMBER: | part347 |
Other MENTHOL; ZINC OXIDE Pharmaceutical Manufacturers / Labelers: