 
                        | Product NDC: | 56062-094 | 
| Proprietary Name: | nasal decongestant pe | 
| Non Proprietary Name: | Phenylephrine Hydrochloride | 
| Active Ingredient(s): | 10 mg/1 & nbsp; Phenylephrine Hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 56062-094 | 
| Labeler Name: | Publix Super Markets Inc | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20050610 | 
| Package NDC: | 56062-094-89 | 
| Package Description: | 1 BLISTER PACK in 1 CARTON (56062-094-89) > 18 TABLET in 1 BLISTER PACK | 
| NDC Code | 56062-094-89 | 
| Proprietary Name | nasal decongestant pe | 
| Package Description | 1 BLISTER PACK in 1 CARTON (56062-094-89) > 18 TABLET in 1 BLISTER PACK | 
| Product NDC | 56062-094 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Phenylephrine Hydrochloride | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20050610 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Publix Super Markets Inc | 
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 10 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |