Surfers Skin Sunscreen (Skin Alive, Ltd.)
Welcome to the PulseAid listing for the Surfers Skin Sunscreen drug offered from Skin Alive, Ltd.. 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: | Skin Alive, Ltd. |
NON-PROPRIETARY NAME: | OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
SUBSTANCE NAME: | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2011-01-31 |
END MARKETING DATE: | 0000-00-00 |
Surfers Skin Sunscreen HUMAN OTC DRUG Details:
Item Description | Surfers Skin Sunscreen from Skin Alive, Ltd. |
LABELER NAME: | Skin Alive, Ltd. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 7.5; 3.45; 1; 1.95(mL/100mL; mL/100mL; mL/100mL; mL/100mL) |
START MARKETING DATE: | 2011-01-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 75916-4019_1bcab3f2-a9fd-4f3a-8f34-528b3223b54c |
PRODUCT NDC: | 75916-4019 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers: