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 Description | SnowSkin 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: