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Mucinex Sinus-Max
Mucinex Sinus-Max - 63824-200-30 - (Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of Mucinex Sinus-Max
| Product NDC: | 63824-200 |
| Proprietary Name: | Mucinex Sinus-Max |
| Non Proprietary Name: | Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 325; 200; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex Sinus-Max
| Product NDC: | 63824-200 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120723 |
Package Information of Mucinex Sinus-Max
| Package NDC: | 63824-200-30 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (63824-200-30) > 10 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Mucinex Sinus-Max
| NDC Code | 63824-200-30 |
| Proprietary Name | Mucinex Sinus-Max |
| Package Description | 3 BLISTER PACK in 1 CARTON (63824-200-30) > 10 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 63824-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120723 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
