Product NDC: | 68391-094 |
Proprietary Name: | Berkley and Jensen 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: | 68391-094 |
Labeler Name: | BJWC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090605 |
Package NDC: | 68391-094-78 |
Package Description: | 1 BOTTLE in 1 CARTON (68391-094-78) > 100 TABLET in 1 BOTTLE |
NDC Code | 68391-094-78 |
Proprietary Name | Berkley and Jensen Nasal Decongestant PE |
Package Description | 1 BOTTLE in 1 CARTON (68391-094-78) > 100 TABLET in 1 BOTTLE |
Product NDC | 68391-094 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Phenylephrine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090605 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | BJWC |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |