SPF 30 Sheer sunscreen faceUlta (Ulta)
Welcome to the PulseAid listing for the SPF 30 Sheer sunscreen face 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 2.00% Homosalate 15.00% Octinoxate 7.50% Octisalate 5.00% |
| SUBSTANCE NAME: | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | STICK |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2016-01-27 |
| END MARKETING DATE: | 0000-00-00 |
SPF 30 Sheer sunscreen face Ulta HUMAN OTC DRUG Details:
| Item Description | SPF 30 Sheer sunscreen face Ulta from Ulta |
| LABELER NAME: | Ulta |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2; 15; 7.5; 5(g/100g; g/100g; g/100g; g/100g) |
| START MARKETING DATE: | 2016-01-27 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62296-7778_5e448a1b-c28b-4ff0-9154-614ee50d5e52 |
| PRODUCT NDC: | 62296-7778 |
| APPLICATION NUMBER: | part352 |
Other AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE Pharmaceutical Manufacturers / Labelers:
