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: |
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| 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:
