SHISEIDO WHITE LUCENT (SHISEIDO AMERICA INC.)
Welcome to the PulseAid listing for the SHISEIDO WHITE LUCENT drug offered from SHISEIDO AMERICA INC.. 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 AMERICA INC. |
| NON-PROPRIETARY NAME: | Octinoxate and Octocrylene |
| SUBSTANCE NAME: | OCTINOXATE; OCTOCRYLENE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | EMULSION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2010-02-01 |
| END MARKETING DATE: | 0000-00-00 |
SHISEIDO WHITE LUCENT HUMAN OTC DRUG Details:
| Item Description | SHISEIDO WHITE LUCENT from SHISEIDO AMERICA INC. |
| LABELER NAME: | SHISEIDO AMERICA INC. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 3.479; 3.55(g/71g; g/71g) |
| START MARKETING DATE: | 2010-02-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 52686-228_c7a40719-a7da-4fe4-b638-a6104d05bd25 |
| PRODUCT NDC: | 52686-228 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:
