SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER (SHISEIDO AMERICAS CORPORATION)
Welcome to the PulseAid listing for the SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER drug offered from SHISEIDO AMERICAS CORPORATION. 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: | SHISEIDO AMERICAS CORPORATION |
NON-PROPRIETARY NAME: | AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
SUBSTANCE NAME: | AVOBENZONE; OCTINOXATE; OCTOCRYLENE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2015-02-01 |
END MARKETING DATE: | 0000-00-00 |
SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER HUMAN OTC DRUG Details:
Item Description | SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER from SHISEIDO AMERICAS CORPORATION |
LABELER NAME: | SHISEIDO AMERICAS CORPORATION |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1273; 3767; 1527(mg/50mL; mg/50mL; mg/50mL) |
START MARKETING DATE: | 2015-02-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 58411-238_cf153a6d-e64a-4d1e-8e98-df1a70d0ec79 |
PRODUCT NDC: | 58411-238 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; OCTINOXATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers: