SUNBAR SPF 15 (Kamins Dermatologics Inc.)
Welcome to the PulseAid listing for the SUNBAR SPF 15 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: | AVOBENZONE HOMOSALATE OCTISALATE OXYBENZONE |
SUBSTANCE NAME: | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | SPRAY |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2010-09-30 |
END MARKETING DATE: | 0000-00-00 |
SUNBAR SPF 15 HUMAN OTC DRUG Details:
Item Description | SUNBAR SPF 15 from Kamins Dermatologics Inc. |
LABELER NAME: | Kamins Dermatologics Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 30; 100; 50; 60(mg/mL; mg/mL; mg/mL; mg/mL) |
START MARKETING DATE: | 2010-09-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63550-810_e20e5f13-95b4-4bfc-9b95-44533d0c533f |
PRODUCT NDC: | 63550-810 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers: