Mucus Relief Congestion and Cough Maximum Strength is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride.
| Product ID | 11673-337_3cbb65ba-cf07-45e4-b7b2-eccb08527b54 |
| NDC | 11673-337 |
| Product Type | Human Otc Drug |
| Proprietary Name | Mucus Relief Congestion and Cough Maximum Strength |
| Generic Name | Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hci |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-07-31 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | TARGET Corporation |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 20 mg/20mL; mg/20mL; mg/20mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2016-07-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-07-31 |
| Ingredient | Strength |
|---|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 20 mg/20mL |
| SPL SET ID: | 1bf9a59e-cc37-4780-ba75-7138c546eb19 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 55316-037 | Mucus Relief Congestion and Cough Maximum Strength | Mucus Relief Congestion and Cough Maximum Strength |
| 11673-337 | Mucus Relief Congestion and Cough | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI |
| 70000-0133 | Tussin | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI |
| 55312-382 | Tussin CF | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI |