Product NDC: | 52904-445 |
Proprietary Name: | Pain Relief PM Nightime Sleep Aid |
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: | 52904-445 |
Labeler Name: | Select Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121015 |
Package NDC: | 52904-445-02 |
Package Description: | 2 TABLET, COATED in 1 PACKET (52904-445-02) |
NDC Code | 52904-445-02 |
Proprietary Name | Pain Relief PM Nightime Sleep Aid |
Package Description | 2 TABLET, COATED in 1 PACKET (52904-445-02) |
Product NDC | 52904-445 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen,Diphenhydramine HCl |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20121015 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Select Corporation |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 500; 25 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |