Neutrogena Blackhead Eliminating Daily Scrub (Johnson & Johnson Consumer Inc.)
Welcome to the PulseAid listing for the Neutrogena Blackhead Eliminating Daily Scrub drug offered from Johnson & Johnson Consumer 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: | Johnson & Johnson Consumer Inc. |
NON-PROPRIETARY NAME: | Salicylic Acid |
SUBSTANCE NAME: | SALICYLIC ACID |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-03-20 |
END MARKETING DATE: | 2018-06-01 |
Neutrogena Blackhead Eliminating Daily Scrub HUMAN OTC DRUG Details:
Item Description | Neutrogena Blackhead Eliminating Daily Scrub from Johnson & Johnson Consumer Inc. |
LABELER NAME: | Johnson & Johnson Consumer Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | 20(mg/mL) |
START MARKETING DATE: | 2012-03-20 |
END MARKETING DATE: | 2018-06-01 |
PRODUCT ID: | 10812-129_d2944aff-4d90-4bfa-adc7-dcdff7c92461 |
PRODUCT NDC: | 10812-129 |
APPLICATION NUMBER: | part333D |