SUNBAR SPF 30 (Kamins Dermatologics Inc.)


Welcome to the PulseAid listing for the SUNBAR SPF 30 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 Octinoxate Oxybenzone Titanium dioxide
SUBSTANCE NAME: AVOBENZONE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2010-10-15
END MARKETING DATE: 0000-00-00


SUNBAR SPF 30 HUMAN OTC DRUG Details:

Item DescriptionSUNBAR SPF 30 from Kamins Dermatologics Inc.
LABELER NAME: Kamins Dermatologics Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 25; 75; 6; 20(mg/mL; mg/mL; mg/mL; mg/mL)
START MARKETING DATE: 2010-10-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63550-811_df11c3bb-6819-4495-baed-c2c9d9baee86
PRODUCT NDC: 63550-811
APPLICATION NUMBER: part352

Other AVOBENZONE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Kamins Dermatologics Inc.SUNBAR SPF 30