SHISEIDO IBUKI MULTI (SHISEIDO AMERICAS CORPORATION)
Welcome to the PulseAid listing for the SHISEIDO IBUKI MULTI 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: | SALICYLIC ACID |
| SUBSTANCE NAME: | SALICYLIC ACID |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | GEL |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2015-02-01 |
| END MARKETING DATE: | 0000-00-00 |
SHISEIDO IBUKI MULTI HUMAN OTC DRUG Details:
| Item Description | SHISEIDO IBUKI MULTI from SHISEIDO AMERICAS CORPORATION |
| LABELER NAME: | SHISEIDO AMERICAS CORPORATION |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | 154(mg/30mL) |
| START MARKETING DATE: | 2015-02-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58411-340_cd4b9d25-f78f-4c35-b6c5-8ce7f3c0f836 |
| PRODUCT NDC: | 58411-340 |
| APPLICATION NUMBER: | part333D |