Derma Soleil Natural Age-Free Facial Sunblock SPF 30 (Derma Soleil)
Welcome to the PulseAid listing for the Derma Soleil Natural Age-Free Facial Sunblock SPF 30 drug offered from Derma Soleil. 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: | Derma Soleil |
| NON-PROPRIETARY NAME: | Octocrylene, Octyl Methoxycinnamate, Octyl Salicylate, Oxybenzone |
| SUBSTANCE NAME: | OCTINOXATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2017-07-20 |
| END MARKETING DATE: | 0000-00-00 |
Derma Soleil Natural Age-Free Facial Sunblock SPF 30 HUMAN OTC DRUG Details:
| Item Description | Derma Soleil Natural Age-Free Facial Sunblock SPF 30 from Derma Soleil |
| LABELER NAME: | Derma Soleil |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 7.5; 4; 5; 4(g/100mL; g/100mL; g/100mL; g/100mL) |
| START MARKETING DATE: | 2017-07-20 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 69711-310_55116052-48e2-555b-e054-00144ff8d46c |
| PRODUCT NDC: | 69711-310 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:
