Product NDC: | 0363-0518 |
Proprietary Name: | Severe Allergy |
Non Proprietary Name: | Acetaminophen and Diphenhydramine HCl |
Active Ingredient(s): | 500; 12.5 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0518 |
Labeler Name: | WALGREEN CO. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20050606 |
Package NDC: | 0363-0518-07 |
Package Description: | 3 BLISTER PACK in 1 CARTON (0363-0518-07) > 12 TABLET in 1 BLISTER PACK |
NDC Code | 0363-0518-07 |
Proprietary Name | Severe Allergy |
Package Description | 3 BLISTER PACK in 1 CARTON (0363-0518-07) > 12 TABLET in 1 BLISTER PACK |
Product NDC | 0363-0518 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen and Diphenhydramine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20050606 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | WALGREEN CO. |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 500; 12.5 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |