Non Drowsy Cold and Cough PE is a Oral Capsule, Coated in the Human Otc Drug category. It is labeled and distributed by Woonsocket Prescription Center,incorporated. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride.
| Product ID | 59779-799_7984e5e8-33f6-4ea1-9937-5a85320c2221 |
| NDC | 59779-799 |
| Product Type | Human Otc Drug |
| Proprietary Name | Non Drowsy Cold and Cough PE |
| Generic Name | Acetaminophen, Dextromathorphan Hbr, Gauifenesin, Phenylephrine Hcl |
| Dosage Form | Capsule, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2007-02-22 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 325 mg/1; mg/1; mg/1; mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2007-02-22 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-02-22 |
| Marketing End Date | 2019-08-21 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-02-22 |
| Marketing End Date | 2019-08-21 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/1 |
| SPL SET ID: | 3a200ba0-6166-44e7-a06d-48820a582d87 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |