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 DescriptionSUN THERAPE BODY SPF-35 from PHARMAGEL INTERNATIONAL INC
LABELER NAME: PHARMAGEL INTERNATIONAL INC
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Bright Guard, LLCBright Guard Water-Resistant SPF-30 Sunscreen
Kingdom Animalia, LLC dba Hourglass ComseticsHourglass Equilibrium Day Fluid
PHARMAGEL INTERNATIONAL INCSUN THERAPE BODY