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Childrens Allergy
Childrens Allergy - 72036-025-04 - (Benadryl)
Drug Information of Childrens Allergy
| Product NDC: | 72036-025 |
| Proprietary Name: | Childrens Allergy |
| Non Proprietary Name: | Benadryl |
| Active Ingredient(s): | 12.5 mg/5mL & nbsp; Benadryl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Allergy
| Product NDC: | 72036-025 |
| Labeler Name: | Harris Teeter |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100119 |
Package Information of Childrens Allergy
| Package NDC: | 72036-025-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (72036-025-04) |
NDC Information of Childrens Allergy
| NDC Code | 72036-025-04 |
| Proprietary Name | Childrens Allergy |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (72036-025-04) |
| Product NDC | 72036-025 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benadryl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100119 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Harris Teeter |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 12.5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
