| 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 |