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MUCUS RELIEF
MUCUS RELIEF - 0904-6232-46 - (GUAIFENESIN)
Drug Information of MUCUS RELIEF
| Product NDC: | 0904-6232 |
| Proprietary Name: | MUCUS RELIEF |
| Non Proprietary Name: | GUAIFENESIN |
| Active Ingredient(s): | 400 mg/1 & nbsp; GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MUCUS RELIEF
| Product NDC: | 0904-6232 |
| Labeler Name: | MAJOR PHARMACEUTICALS INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120723 |
Package Information of MUCUS RELIEF
| Package NDC: | 0904-6232-46 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (0904-6232-46) |
NDC Information of MUCUS RELIEF
| NDC Code | 0904-6232-46 |
| Proprietary Name | MUCUS RELIEF |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (0904-6232-46) |
| Product NDC | 0904-6232 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120723 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MAJOR PHARMACEUTICALS INC |
| Substance Name | GUAIFENESIN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
