DerMend Moisturizing Anti-Itch (Ferndale Laboratories, Inc.)
Welcome to the PulseAid listing for the DerMend Moisturizing Anti-Itch drug offered from Ferndale Laboratories, 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: | Ferndale Laboratories, Inc. |
| NON-PROPRIETARY NAME: | pramoxine hydrochloride |
| SUBSTANCE NAME: | PRAMOXINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2017-03-01 |
| END MARKETING DATE: | 0000-00-00 |
DerMend Moisturizing Anti-Itch HUMAN OTC DRUG Details:
| Item Description | DerMend Moisturizing Anti-Itch from Ferndale Laboratories, Inc. |
| LABELER NAME: | Ferndale Laboratories, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2017-03-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0496-0586_48814a87-ee9c-2e5b-e054-00144ff8d46c |
| PRODUCT NDC: | 0496-0586 |
| APPLICATION NUMBER: | part348 |
Other PRAMOXINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
