ULTA Sunscreen SPF 30 (Ulta)
Welcome to the PulseAid listing for the ULTA Sunscreen SPF 30 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: | AVOBENZONE, HOMOSALATE, OCTOCRYLENE |
SUBSTANCE NAME: | AVOBENZONE; HOMOSALATE; OCTOCRYLENE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2015-08-11 |
END MARKETING DATE: | 0000-00-00 |
ULTA Sunscreen SPF 30 HUMAN OTC DRUG Details:
Item Description | ULTA Sunscreen SPF 30 from Ulta |
LABELER NAME: | Ulta |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 1.8; 7; 5(g/100g; g/100g; g/100g) |
START MARKETING DATE: | 2015-08-11 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62296-2273_70d6a95f-a43f-4ce5-9439-aca04e5db586 |
PRODUCT NDC: | 62296-2273 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; HOMOSALATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers: