DR. WALTONSBABY POWDER (Dr. Waltons, Incorporated)
Welcome to the PulseAid listing for the DR. WALTONS drug offered from Dr. Waltons, Incorporated. 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: | Dr. Waltons, Incorporated |
| NON-PROPRIETARY NAME: | TALC |
| SUBSTANCE NAME: | ALPHA-TOCOPHEROL; ZINC OXIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | POWDER |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2011-07-09 |
| END MARKETING DATE: | 0000-00-00 |
DR. WALTONS BABY POWDER HUMAN OTC DRUG Details:
| Item Description | DR. WALTONS BABY POWDER from Dr. Waltons, Incorporated |
| LABELER NAME: | Dr. Waltons, Incorporated |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5.2; 5.13(g/675g; g/675g) |
| START MARKETING DATE: | 2011-07-09 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 76271-001_c6e98d27-268e-4ab6-98d6-746b45d4c56c |
| PRODUCT NDC: | 76271-001 |
| APPLICATION NUMBER: | part347 |
Other ALPHA-TOCOPHEROL; ZINC OXIDE Pharmaceutical Manufacturers / Labelers:
