SUNSCREEN MOISTURIZERSPF 30 (Skin Authority LLC)


Welcome to the PulseAid listing for the SUNSCREEN MOISTURIZER drug offered from Skin Authority LLC. 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: Skin Authority LLC
NON-PROPRIETARY NAME: AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE
SUBSTANCE NAME: AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE; HOMOSALATE; OCTOCRYLENE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2012-04-19
END MARKETING DATE: 0000-00-00


SUNSCREEN MOISTURIZER SPF 30 HUMAN OTC DRUG Details:

Item DescriptionSUNSCREEN MOISTURIZER SPF 30 from Skin Authority LLC
LABELER NAME: Skin Authority LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 7.5; 5; 6; 7; 3(g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL)
START MARKETING DATE: 2012-04-19
END MARKETING DATE: 0000-00-00
PRODUCT ID: 46007-203_0f90b87f-9aba-456f-b785-1a6b0e311f09
PRODUCT NDC: 46007-203
APPLICATION NUMBER: part352

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

Manufacturer / LabelerProprietary Name
Skin Authority LLCAGE DEFYING HYDRATING SUNSCREEN