Snowberry (Snowberry New Zealand Ltd)
Welcome to the PulseAid listing for the Snowberry drug offered from Snowberry New Zealand Ltd. 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: | Snowberry New Zealand Ltd |
| NON-PROPRIETARY NAME: | Zinc Oxide |
| SUBSTANCE NAME: | ZINC OXIDE; KAEMPFERIA GALANGA ROOT; ETHYL FERULATE; LARIX SIBIRICA WOOD |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2013-04-01 |
| END MARKETING DATE: | 0000-00-00 |
Snowberry HUMAN OTC DRUG Details:
| Item Description | Snowberry from Snowberry New Zealand Ltd |
| LABELER NAME: | Snowberry New Zealand Ltd |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 1.6; .7; .7; .3(g/10g; g/10g; g/10g; g/10g) |
| START MARKETING DATE: | 2013-04-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58231-001_4d01bfba-2dd9-4951-a761-8aa6f4f697bc |
| PRODUCT NDC: | 58231-001 |
| APPLICATION NUMBER: | part352 |
Other ZINC OXIDE; KAEMPFERIA GALANGA ROOT; ETHYL FERULATE; LARIX SIBIRICA WOOD Pharmaceutical Manufacturers / Labelers:
