SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER N (SHISEIDO AMERICAS CORPORATION)
Welcome to the PulseAid listing for the SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER N 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, OCTOCRYLENE, and OXYBENZONE |
| SUBSTANCE NAME: | AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2017-02-01 |
| END MARKETING DATE: | 0000-00-00 |
SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER N HUMAN OTC DRUG Details:
| Item Description | SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER N from SHISEIDO AMERICAS CORPORATION |
| LABELER NAME: | SHISEIDO AMERICAS CORPORATION |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1283; 3796; 1539; 513(mg/50mL; mg/50mL; mg/50mL; mg/50mL) |
| START MARKETING DATE: | 2017-02-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58411-295_7b83886b-dce9-4b2e-9c3d-46dfd98c4a24 |
| PRODUCT NDC: | 58411-295 |
| APPLICATION NUMBER: | part352 |
Other AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:
