Ultra Glow Fadewith Aloe Vera (Keystone Laboratories)
Welcome to the PulseAid listing for the Ultra Glow Fade drug offered from Keystone Laboratories. 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: | Keystone Laboratories |
| NON-PROPRIETARY NAME: | Hydroquinone, Padimate O |
| SUBSTANCE NAME: | HYDROQUINONE; PADIMATE O |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 1964-04-07 |
| END MARKETING DATE: | 0000-00-00 |
Ultra Glow Fade with Aloe Vera HUMAN OTC DRUG Details:
| Item Description | Ultra Glow Fade with Aloe Vera from Keystone Laboratories |
| LABELER NAME: | Keystone Laboratories |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1; 1(g/57g; g/57g) |
| START MARKETING DATE: | 1964-04-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58318-002_3a988b2a-78e4-4250-bb4a-670403b086e1 |
| PRODUCT NDC: | 58318-002 |
| APPLICATION NUMBER: | part358A |
Other HYDROQUINONE; PADIMATE O Pharmaceutical Manufacturers / Labelers:
