ZO MEDICAL SURFATROL Astringent (ZO Skin Health, Inc.)
Welcome to the PulseAid listing for the ZO MEDICAL SURFATROL Astringent drug offered from ZO Skin Health, 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: | ZO Skin Health, Inc. |
| NON-PROPRIETARY NAME: | Aluminum Acetate |
| SUBSTANCE NAME: | ALUMINUM ACETATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | POWDER |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2016-08-01 |
| END MARKETING DATE: | 0000-00-00 |
ZO MEDICAL SURFATROL Astringent HUMAN OTC DRUG Details:
| Item Description | ZO MEDICAL SURFATROL Astringent from ZO Skin Health, Inc. |
| LABELER NAME: | ZO Skin Health, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 4866(mg/4.866g) |
| START MARKETING DATE: | 2016-08-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 42851-084_af2e1f39-b312-41f4-923c-18a4dff99e1f |
| PRODUCT NDC: | 42851-084 |
| APPLICATION NUMBER: | part347 |
Other ALUMINUM ACETATE Pharmaceutical Manufacturers / Labelers:
