ULTA TANNING SPF 4 (Ulta)
Welcome to the PulseAid listing for the ULTA TANNING SPF 4 drug offered from Ulta. 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: | Ulta |
NON-PROPRIETARY NAME: | Octinoxate, Padimate O |
SUBSTANCE NAME: | OCTINOXATE; PADIMATE O |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2015-08-03 |
END MARKETING DATE: | 0000-00-00 |
ULTA TANNING SPF 4 HUMAN OTC DRUG Details:
Item Description | ULTA TANNING SPF 4 from Ulta |
LABELER NAME: | Ulta |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 2; 1.4(g/100g; g/100g) |
START MARKETING DATE: | 2015-08-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62296-7031_b909a65b-a935-4cbe-9e06-e0c2882ed020 |
PRODUCT NDC: | 62296-7031 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; PADIMATE O Pharmaceutical Manufacturers / Labelers: