| Product NDC: | 0573-0167 |
| Proprietary Name: | ADVIL PM |
| Non Proprietary Name: | diphenhydramine HCl, ibuprofen |
| Active Ingredient(s): | 25; 200 mg/1; mg/1 & nbsp; diphenhydramine HCl, ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0573-0167 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021393 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051220 |
| Package NDC: | 0573-0167-10 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0573-0167-10) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| NDC Code | 0573-0167-10 |
| Proprietary Name | ADVIL PM |
| Package Description | 2 BLISTER PACK in 1 CARTON (0573-0167-10) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 0573-0167 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine HCl, ibuprofen |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20051220 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN |
| Strength Number | 25; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |