| Product NDC: | 49035-527 |
| Proprietary Name: | Severe Sinus Congestion and Pain |
| Non Proprietary Name: | Aceetaminophen, Guaifenesin and Phenylephrine HCl |
| Active Ingredient(s): | 325; 200; 5 mg/1; mg/1; mg/1 & nbsp; Aceetaminophen, Guaifenesin and Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49035-527 |
| Labeler Name: | Wal-Mart Stores Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050806 |
| Package NDC: | 49035-527-08 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (49035-527-08) > 24 TABLET in 1 BLISTER PACK |
| NDC Code | 49035-527-08 |
| Proprietary Name | Severe Sinus Congestion and Pain |
| Package Description | 1 BLISTER PACK in 1 CARTON (49035-527-08) > 24 TABLET in 1 BLISTER PACK |
| Product NDC | 49035-527 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aceetaminophen, Guaifenesin and Phenylephrine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050806 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Wal-Mart Stores Inc |
| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |