 
                        | Product NDC: | 68016-235 | 
| Proprietary Name: | Nasal Decongestant | 
| Non Proprietary Name: | Phenylephrine HCl | 
| Active Ingredient(s): | 10 mg/1 & nbsp; Phenylephrine HCl | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 68016-235 | 
| Labeler Name: | Chain Drug Consortium, LLC (Premier Value) | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20100712 | 
| Package NDC: | 68016-235-15 | 
| Package Description: | 2 BLISTER PACK in 1 CARTON (68016-235-15) > 18 TABLET in 1 BLISTER PACK | 
| NDC Code | 68016-235-15 | 
| Proprietary Name | Nasal Decongestant | 
| Package Description | 2 BLISTER PACK in 1 CARTON (68016-235-15) > 18 TABLET in 1 BLISTER PACK | 
| Product NDC | 68016-235 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Phenylephrine HCl | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20100712 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Chain Drug Consortium, LLC (Premier Value) | 
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 10 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |