Face and Body Sunscreen SpraySPF 35 (Jafra Cosmetics International Inc)


Welcome to the PulseAid listing for the Face and Body Sunscreen Spray drug offered from Jafra Cosmetics 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: Jafra Cosmetics International Inc
NON-PROPRIETARY NAME: Homosalate, Oxybenzone, Octinoxate, Octisalate, Octocrylene
SUBSTANCE NAME: HOMOSALATE; OCTINOXATE; OXYBENZONE; OCTISALATE; OCTOCRYLENE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2012-06-05
END MARKETING DATE: 0000-00-00


Face and Body Sunscreen Spray SPF 35 HUMAN OTC DRUG Details:

Item DescriptionFace and Body Sunscreen Spray SPF 35 from Jafra Cosmetics International Inc
LABELER NAME: Jafra Cosmetics International Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 10; 3; 6; 5; 2.79(mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL)
START MARKETING DATE: 2012-06-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68828-092_20684ed5-35c3-4aaf-a2a5-1be32741fc6b
PRODUCT NDC: 68828-092
APPLICATION NUMBER: part352

Other HOMOSALATE; OCTINOXATE; OXYBENZONE; OCTISALATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Jafra Cosmetics International IncFace and Body Sunscreen Spray