| Product NDC: | 68016-021 | 
| Proprietary Name: | Premier Value Chest and Sinus Congestion relief | 
| Non Proprietary Name: | Guaifenesin/phenylephrine | 
| Active Ingredient(s): | 400; 10 mg/1; mg/1 & nbsp; Guaifenesin/phenylephrine | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 68016-021 | 
| Labeler Name: | Premier Value | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20060201 | 
| Package NDC: | 68016-021-01 | 
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (68016-021-01) > 50 TABLET in 1 BOTTLE, PLASTIC (68016-021-07) | 
| NDC Code | 68016-021-01 | 
| Proprietary Name | Premier Value Chest and Sinus Congestion relief | 
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (68016-021-01) > 50 TABLET in 1 BOTTLE, PLASTIC (68016-021-07) | 
| Product NDC | 68016-021 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Guaifenesin/phenylephrine | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20060201 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Premier Value | 
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 400; 10 | 
| Strength Unit | mg/1; mg/1 | 
| Pharmaceutical Classes |