SunBum SPF 50 (Sun Bum)


Welcome to the PulseAid listing for the SunBum SPF 50 drug offered from Sun Bum. 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: Sun Bum
NON-PROPRIETARY NAME: Octisalate – 5.00% Octinoxate – 7.50% Oxybenzone – 6.00% Zinc Oxide – 7.00%
SUBSTANCE NAME: OCTISALATE; OCTINOXATE; OXYBENZONE; ZINC OXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2011-02-10
END MARKETING DATE: 0000-00-00


SunBum SPF 50 HUMAN OTC DRUG Details:

Item DescriptionSunBum SPF 50 from Sun Bum
LABELER NAME: Sun Bum
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 7.5; 6; 7(g/100mL; g/100mL; g/100mL; 1/100mL)
START MARKETING DATE: 2011-02-10
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69039-559_2a2eae98-efeb-4b3e-9ce7-6ad972364280
PRODUCT NDC: 69039-559
APPLICATION NUMBER: part352

Other OCTISALATE; OCTINOXATE; OXYBENZONE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Sun BumSunBum SPF 50