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Mucus Relief PE
Mucus Relief PE - 21130-542-01 - (Guaifenesin and Phenylephrine HCl)
Drug Information of Mucus Relief PE
| Product NDC: | 21130-542 |
| Proprietary Name: | Mucus Relief PE |
| Non Proprietary Name: | Guaifenesin and Phenylephrine HCl |
| Active Ingredient(s): | 400; 10 mg/1; mg/1 & nbsp; Guaifenesin and Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucus Relief PE
| Product NDC: | 21130-542 |
| Labeler Name: | Safeway |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060415 |
Package Information of Mucus Relief PE
| Package NDC: | 21130-542-01 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (21130-542-01) > 30 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Mucus Relief PE
| NDC Code | 21130-542-01 |
| Proprietary Name | Mucus Relief PE |
| Package Description | 1 BLISTER PACK in 1 CARTON (21130-542-01) > 30 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 21130-542 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Phenylephrine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20060415 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Safeway |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 400; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
