ULTA FACE SPF 30 (Ulta)
Welcome to the PulseAid listing for the ULTA FACE 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, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
SUBSTANCE NAME: | AVOBENZONE; HOMOSALATE; OCTOCRYLENE; OCTISALATE; OXYBENZONE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2015-08-17 |
END MARKETING DATE: | 0000-00-00 |
ULTA FACE SPF 30 HUMAN OTC DRUG Details:
Item Description | ULTA FACE SPF 30 from Ulta |
LABELER NAME: | Ulta |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2; 13; 2; 5; 4(g/100g; g/100g; g/100g; g/100g; g/100g) |
START MARKETING DATE: | 2015-08-17 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62296-8292_d45165d4-d9aa-427b-b338-0512db3b2a4e |
PRODUCT NDC: | 62296-8292 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; HOMOSALATE; OCTOCRYLENE; OCTISALATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers: