 
                        | Product NDC: | 42507-432 | 
| Proprietary Name: | nasal decongestant | 
| Non Proprietary Name: | Pseudoephedrine HCl | 
| Active Ingredient(s): | 30 mg/1 & nbsp; Pseudoephedrine HCl | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 42507-432 | 
| Labeler Name: | HyVee Inc | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 19890115 | 
| Package NDC: | 42507-432-62 | 
| Package Description: | 1 BLISTER PACK in 1 CARTON (42507-432-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK | 
| NDC Code | 42507-432-62 | 
| Proprietary Name | nasal decongestant | 
| Package Description | 1 BLISTER PACK in 1 CARTON (42507-432-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK | 
| Product NDC | 42507-432 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Pseudoephedrine HCl | 
| Dosage Form Name | TABLET, FILM COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 19890115 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | HyVee Inc | 
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE | 
| Strength Number | 30 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |