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 DescriptionSunbar SPF 48 from Kamins Dermatologics Inc.
LABELER NAME: Kamins Dermatologics Inc.
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Kamins Dermatologics Inc.Sunbar SPF 48