SnowSkin Face Sunscreen (Skin Alive, Ltd.)


Welcome to the PulseAid listing for the SnowSkin Face Sunscreen drug offered from Skin Alive, Ltd.. 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 Alive, Ltd.
NON-PROPRIETARY NAME: OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE
SUBSTANCE NAME: OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: STICK
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2011-01-17
END MARKETING DATE: 0000-00-00


SnowSkin Face Sunscreen HUMAN OTC DRUG Details:

Item DescriptionSnowSkin Face Sunscreen from Skin Alive, Ltd.
LABELER NAME: Skin Alive, Ltd.
DEA SCHEDULE:
ACTIVE STRENGTH: 6; 3.3; 14.25(g/100g; g/100g; g/100g)
START MARKETING DATE: 2011-01-17
END MARKETING DATE: 0000-00-00
PRODUCT ID: 75916-0641_526a2a52-0b3b-4664-816e-537b0783946c
PRODUCT NDC: 75916-0641
APPLICATION NUMBER: part352

Other OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Skin Alive, Ltd.SnowSkin Face Sunscreen