Sunmark Redness Relief (McKesson Corporation)
Welcome to the PulseAid listing for the Sunmark Redness Relief drug offered from McKesson 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: | McKesson Corporation |
| NON-PROPRIETARY NAME: | Glycerin, Naphazoline hydrochloride |
| SUBSTANCE NAME: | GLYCERIN; NAPHAZOLINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | LIQUID |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2009-10-01 |
| END MARKETING DATE: | 0000-00-00 |
Sunmark Redness Relief HUMAN OTC DRUG Details:
| Item Description | Sunmark Redness Relief from McKesson Corporation |
| LABELER NAME: | McKesson Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | .2; .012(g/100mL; g/100mL) |
| START MARKETING DATE: | 2009-10-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49348-894_117ea02b-a6ac-4bf4-bb54-52489b58dbc4 |
| PRODUCT NDC: | 49348-894 |
| APPLICATION NUMBER: | part349 |
Other GLYCERIN; NAPHAZOLINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: