TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT (Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)
Welcome to the PulseAid listing for the TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT drug offered from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division. 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., McNeil Consumer Healthcare Division |
| NON-PROPRIETARY NAME: | acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2016-07-18 |
| END MARKETING DATE: | 0000-00-00 |
TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT HUMAN OTC DRUG Details:
| Item Description | TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| LABELER NAME: | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2016-07-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50580-414_9917caf1-5e27-4634-b56c-dce1218de48d |
| PRODUCT NDC: | 50580-414 |
| APPLICATION NUMBER: | part341 |