Sinex (The Procter & Gamble Manufacturing Company)
Welcome to the PulseAid listing for the Sinex drug offered from The Procter & Gamble Manufacturing Company. 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: | The Procter & Gamble Manufacturing Company |
NON-PROPRIETARY NAME: | Acetaminophen, Doxylamine succinate, and Phenylephrine hydrochloride |
SUBSTANCE NAME: | ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE, LIQUID FILLED |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2016-07-29 |
END MARKETING DATE: | 0000-00-00 |
Sinex HUMAN OTC DRUG Details:
Item Description | Sinex from The Procter & Gamble Manufacturing Company |
LABELER NAME: | The Procter & Gamble Manufacturing Company |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 325; 6.25; 5(mg/1; mg/1; mg/1) |
START MARKETING DATE: | 2016-07-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 37000-508_56b811e6-774d-2882-e054-00144ff8d46c |
PRODUCT NDC: | 37000-508 |
APPLICATION NUMBER: | part341 |
Other ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: