Sunmark Hemorrhoidal (McKesson)
Welcome to the PulseAid listing for the Sunmark Hemorrhoidal drug offered from McKesson. 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: | McKesson |
NON-PROPRIETARY NAME: | glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum |
SUBSTANCE NAME: | GLYCERIN; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE; PETROLATUM |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2008-02-04 |
END MARKETING DATE: | 0000-00-00 |
Sunmark Hemorrhoidal HUMAN OTC DRUG Details:
Item Description | Sunmark Hemorrhoidal from McKesson |
LABELER NAME: | McKesson |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 14.4; .25; 1; 15(g/100g; g/100g; g/100g; g/100g) |
START MARKETING DATE: | 2008-02-04 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49348-799_a101cfad-fa2e-4bd4-8cee-d66e3d3e5438 |
PRODUCT NDC: | 49348-799 |
APPLICATION NUMBER: | part346 |
Other GLYCERIN; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE; PETROLATUM Pharmaceutical Manufacturers / Labelers: