| Product NDC: | 62011-0024 |
| Proprietary Name: | Extra Strength Acetaminophen PM |
| Non Proprietary Name: | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62011-0024 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120409 |
| Package NDC: | 62011-0024-1 |
| Package Description: | 1 BOTTLE in 1 BOX (62011-0024-1) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| NDC Code | 62011-0024-1 |
| Proprietary Name | Extra Strength Acetaminophen PM |
| Package Description | 1 BOTTLE in 1 BOX (62011-0024-1) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 62011-0024 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20120409 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McKesson |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |