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 Description | SunBum SPF 50 from Sun Bum |
LABELER NAME: | Sun Bum |
DEA SCHEDULE: |
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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: