Sunmark Benzoin Compound Tincture (McKesson)
Welcome to the PulseAid listing for the Sunmark Benzoin Compound Tincture 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: | Benzoin Resin |
| SUBSTANCE NAME: | BENZOIN RESIN |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LIQUID |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2008-01-01 |
| END MARKETING DATE: | 0000-00-00 |
Sunmark Benzoin Compound Tincture HUMAN OTC DRUG Details:
| Item Description | Sunmark Benzoin Compound Tincture from McKesson |
| LABELER NAME: | McKesson |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1000(mg/mL) |
| START MARKETING DATE: | 2008-01-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49348-138_6d414111-ad02-4d2e-a138-9e76f1042cae |
| PRODUCT NDC: | 49348-138 |
| APPLICATION NUMBER: | part356 |
Other BENZOIN RESIN Pharmaceutical Manufacturers / Labelers:
