SUN THERAPE BODYSPF-35 (PHARMAGEL INTERNATIONAL INC)
Welcome to the PulseAid listing for the SUN THERAPE BODY drug offered from PHARMAGEL INTERNATIONAL 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: | PHARMAGEL INTERNATIONAL INC |
NON-PROPRIETARY NAME: | HOMOSALATE, OCTINOXATE, OCTISALATE, AVOBENZONE |
SUBSTANCE NAME: | HOMOSALATE; OCTINOXATE; OCTISALATE; AVOBENZONE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2015-06-18 |
END MARKETING DATE: | 0000-00-00 |
SUN THERAPE BODY SPF-35 HUMAN OTC DRUG Details:
Item Description | SUN THERAPE BODY SPF-35 from PHARMAGEL INTERNATIONAL INC |
LABELER NAME: | PHARMAGEL INTERNATIONAL INC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10; 7.5; 5; 3(g/100mL; g/100mL; g/100mL; g/100mL) |
START MARKETING DATE: | 2015-06-18 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 67879-303_0811eb1d-a929-4f85-aea2-ec427eb4550b |
PRODUCT NDC: | 67879-303 |
APPLICATION NUMBER: | part352 |
Other HOMOSALATE; OCTINOXATE; OCTISALATE; AVOBENZONE Pharmaceutical Manufacturers / Labelers: