SoftlipsVanilla (The Mentholatum Company)
Welcome to the PulseAid listing for the Softlips drug offered from The Mentholatum Company. 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: | The Mentholatum Company |
| NON-PROPRIETARY NAME: | dimethicone, octinoxate, octisalate, oxybenzone |
| SUBSTANCE NAME: | DIMETHICONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | OINTMENT |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 1997-11-19 |
| END MARKETING DATE: | 0000-00-00 |
Softlips Vanilla HUMAN OTC DRUG Details:
| Item Description | Softlips Vanilla from The Mentholatum Company |
| LABELER NAME: | The Mentholatum Company |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20; 75; 30; 30(mg/g; mg/g; mg/g; mg/g) |
| START MARKETING DATE: | 1997-11-19 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 10742-3051_1069f411-4a70-4409-905d-2ebc6b9b4ec5 |
| PRODUCT NDC: | 10742-3051 |
| APPLICATION NUMBER: | part352 |
Other DIMETHICONE; OCTINOXATE; OCTISALATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:
