Everyday Sunscreen SPF 50Supergoop (TAYLOR JAMES, LTD.)
Welcome to the PulseAid listing for the Everyday Sunscreen SPF 50 drug offered from TAYLOR JAMES, 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: | TAYLOR JAMES, LTD. |
NON-PROPRIETARY NAME: | Avobenzone, Homosalate, Octinoxate, Octisalate |
SUBSTANCE NAME: | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2015-01-20 |
END MARKETING DATE: | 0000-00-00 |
Everyday Sunscreen SPF 50 Supergoop HUMAN OTC DRUG Details:
Item Description | Everyday Sunscreen SPF 50 Supergoop from TAYLOR JAMES, LTD. |
LABELER NAME: | TAYLOR JAMES, LTD. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3; 10; 7.5; 5(g/100mL; g/100mL; g/100mL; g/100mL) |
START MARKETING DATE: | 2015-01-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 75936-135_3bb571a8-4e7c-4431-ab8e-f797560be9f6 |
PRODUCT NDC: | 75936-135 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE Pharmaceutical Manufacturers / Labelers: