Product NDC: | 41167-0040 |
Proprietary Name: | Unisom PM Pain Nighttime Sleep Aid and Pain Reliever |
Non Proprietary Name: | Acetaminophen and Diphenhydramine Hydrochloride |
Active Ingredient(s): | 325; 50 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41167-0040 |
Labeler Name: | Chattem, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part338 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091201 |
Package NDC: | 41167-0040-3 |
Package Description: | 1 BOTTLE in 1 CARTON (41167-0040-3) > 20 TABLET in 1 BOTTLE |
NDC Code | 41167-0040-3 |
Proprietary Name | Unisom PM Pain Nighttime Sleep Aid and Pain Reliever |
Package Description | 1 BOTTLE in 1 CARTON (41167-0040-3) > 20 TABLET in 1 BOTTLE |
Product NDC | 41167-0040 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen and Diphenhydramine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Chattem, Inc. |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 325; 50 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |