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: | Octinoxate – 7.50% Octisalate – 5.00% Octocrylene – 7.00% Zinc Oxide – 10.00% |
SUBSTANCE NAME: | OCTINOXATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2015-01-22 |
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: | 7.5; 5; 7; 10(g/100mL; g/100mL; g/100mL; 1/100mL) |
START MARKETING DATE: | 2015-01-22 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69039-558_1b0c02e2-f973-4933-8da0-3eb0b5e00a48 |
PRODUCT NDC: | 69039-558 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers: