Product NDC: | 49035-599 |
Proprietary Name: | Childrens Allergy Relief |
Non Proprietary Name: | Diphenhydramine |
Active Ingredient(s): | 12.5 mg/1 & nbsp; Diphenhydramine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49035-599 |
Labeler Name: | Wal-Mart Stores Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110501 |
Package NDC: | 49035-599-44 |
Package Description: | 1 BLISTER PACK in 1 CARTON (49035-599-44) > 18 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Code | 49035-599-44 |
Proprietary Name | Childrens Allergy Relief |
Package Description | 1 BLISTER PACK in 1 CARTON (49035-599-44) > 18 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
Product NDC | 49035-599 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 20110501 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Wal-Mart Stores Inc |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 12.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |