sunscreen (Humphreyline)
Welcome to the PulseAid listing for the sunscreen drug offered from Humphreyline. 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: | Humphreyline |
| NON-PROPRIETARY NAME: | octinoxate, octisalate, octocrylene, oxybenzone |
| SUBSTANCE NAME: | OCTINOXATE; OXYBENZONE; OCTISALATE; OCTOCRYLENE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2010-01-01 |
| END MARKETING DATE: | 0000-00-00 |
sunscreen HUMAN OTC DRUG Details:
| Item Description | sunscreen from Humphreyline |
| LABELER NAME: | Humphreyline |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 65; 55; 40; 70(mg/g; mg/g; mg/g; mg/g) |
| START MARKETING DATE: | 2010-01-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 19392-400_34817253-7264-43a8-bcaa-1258a75ba993 |
| PRODUCT NDC: | 19392-400 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OXYBENZONE; OCTISALATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:
