Bengay Ultra Strength Pain RelievingRegular Size (Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.)
Welcome to the PulseAid listing for the Bengay Ultra Strength Pain Relieving drug offered from Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, 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 Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
NON-PROPRIETARY NAME: | Menthol |
SUBSTANCE NAME: | MENTHOL |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | PATCH |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2011-09-22 |
END MARKETING DATE: | 0000-00-00 |
Bengay Ultra Strength Pain Relieving Regular Size HUMAN OTC DRUG Details:
Item Description | Bengay Ultra Strength Pain Relieving Regular Size from Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
LABELER NAME: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | 50(mg/1) |
START MARKETING DATE: | 2011-09-22 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 58232-4026_56eba23a-0261-4eb9-821c-2ec661f0caca |
PRODUCT NDC: | 58232-4026 |
APPLICATION NUMBER: | part348 |