Sunbar SPF 48 (Kamins Dermatologics Inc.)
Welcome to the PulseAid listing for the Sunbar SPF 48 drug offered from Kamins Dermatologics Inc.. 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: | Kamins Dermatologics Inc. |
NON-PROPRIETARY NAME: | Ensulizole Homosalate Octinoxate Octocrylene Zinc oxide |
SUBSTANCE NAME: | ENSULIZOLE; HOMOSALATE; OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2010-09-29 |
END MARKETING DATE: | 0000-00-00 |
Sunbar SPF 48 HUMAN OTC DRUG Details:
Item Description | Sunbar SPF 48 from Kamins Dermatologics Inc. |
LABELER NAME: | Kamins Dermatologics Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 30; 100; 75; 70; 80(mg/mL; mg/mL; mg/mL; mg/mL; mg/mL) |
START MARKETING DATE: | 2010-09-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63550-809_30b4cbbf-d534-4fca-9e49-05738ba8e688 |
PRODUCT NDC: | 63550-809 |
APPLICATION NUMBER: | part352 |
Other ENSULIZOLE; HOMOSALATE; OCTINOXATE; OCTOCRYLENE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers: