| Product NDC: | 59640-025 | 
| Proprietary Name: | Childrens Allergy | 
| Non Proprietary Name: | Diphenhydramine Hydrochloride | 
| Active Ingredient(s): | 12.5 mg/5mL & nbsp; Diphenhydramine Hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59640-025 | 
| Labeler Name: | H.E.B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20100302 | 
| Package NDC: | 59640-025-08 | 
| Package Description: | 237 mL in 1 BOTTLE, PLASTIC (59640-025-08) | 
| NDC Code | 59640-025-08 | 
| Proprietary Name | Childrens Allergy | 
| Package Description | 237 mL in 1 BOTTLE, PLASTIC (59640-025-08) | 
| Product NDC | 59640-025 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Diphenhydramine Hydrochloride | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20100302 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H.E.B | 
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE | 
| Strength Number | 12.5 | 
| Strength Unit | mg/5mL | 
| Pharmaceutical Classes |