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Mucus Relief Plus
Mucus Relief Plus - 0363-0372-01 - (Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl)
Drug Information of Mucus Relief Plus
| Product NDC: | 0363-0372 |
| Proprietary Name: | Mucus Relief Plus |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Active Ingredient(s): | 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucus Relief Plus
| Product NDC: | 0363-0372 |
| Labeler Name: | WALGREEN CO. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20020727 |
Package Information of Mucus Relief Plus
| Package NDC: | 0363-0372-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (0363-0372-01) > 30 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of Mucus Relief Plus
| NDC Code | 0363-0372-01 |
| Proprietary Name | Mucus Relief Plus |
| Package Description | 1 BOTTLE in 1 CARTON (0363-0372-01) > 30 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 0363-0372 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020727 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | WALGREEN CO. |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
