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Benadryl Extra Strength
Benadryl Extra Strength - 58232-0741-1 - (Diphenhydramine Hydrochloride and Zinc Acetate)
Drug Information of Benadryl Extra Strength
| Product NDC: | 58232-0741 |
| Proprietary Name: | Benadryl Extra Strength |
| Non Proprietary Name: | Diphenhydramine Hydrochloride and Zinc Acetate |
| Active Ingredient(s): | 2; 1 mg/g; mg/g & nbsp; Diphenhydramine Hydrochloride and Zinc Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benadryl Extra Strength
| Product NDC: | 58232-0741 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121015 |
Package Information of Benadryl Extra Strength
| Package NDC: | 58232-0741-1 |
| Package Description: | 1 TUBE in 1 CARTON (58232-0741-1) > 28.3 g in 1 TUBE |
NDC Information of Benadryl Extra Strength
| NDC Code | 58232-0741-1 |
| Proprietary Name | Benadryl Extra Strength |
| Package Description | 1 TUBE in 1 CARTON (58232-0741-1) > 28.3 g in 1 TUBE |
| Product NDC | 58232-0741 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride and Zinc Acetate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 2; 1 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
