| Product NDC: | 68391-161 | 
| Proprietary Name: | Acetaminophen PM | 
| Non Proprietary Name: | Acetaminophen, Diphenhydramine HCl | 
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine HCl | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 68391-161 | 
| Labeler Name: | BJWC (Berkley & Jensen / BJ's) | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part343 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20130115 | 
| Package NDC: | 68391-161-05 | 
| Package Description: | 500 TABLET, COATED in 1 BOTTLE (68391-161-05) | 
| NDC Code | 68391-161-05 | 
| Proprietary Name | Acetaminophen PM | 
| Package Description | 500 TABLET, COATED in 1 BOTTLE (68391-161-05) | 
| Product NDC | 68391-161 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Diphenhydramine HCl | 
| Dosage Form Name | TABLET, COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 20130115 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | BJWC (Berkley & Jensen / BJ's) | 
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 
| Strength Number | 500; 25 | 
| Strength Unit | mg/1; mg/1 | 
| Pharmaceutical Classes |