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Extra Strength BENADRYL Itch Cooling
Extra Strength BENADRYL Itch Cooling - 58232-0750-2 - (Diphenhydramine Hydrochloride and Zinc Acetate)
Drug Information of Extra Strength BENADRYL Itch Cooling
| Product NDC: | 58232-0750 |
| Proprietary Name: | Extra Strength BENADRYL Itch Cooling |
| Non Proprietary Name: | Diphenhydramine Hydrochloride and Zinc Acetate |
| Active Ingredient(s): | 20; 1 mg/mL; mg/mL & nbsp; Diphenhydramine Hydrochloride and Zinc Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Extra Strength BENADRYL Itch Cooling
| Product NDC: | 58232-0750 |
| 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: | 20120322 |
Package Information of Extra Strength BENADRYL Itch Cooling
| Package NDC: | 58232-0750-2 |
| Package Description: | 59 mL in 1 BOTTLE, SPRAY (58232-0750-2) |
NDC Information of Extra Strength BENADRYL Itch Cooling
| NDC Code | 58232-0750-2 |
| Proprietary Name | Extra Strength BENADRYL Itch Cooling |
| Package Description | 59 mL in 1 BOTTLE, SPRAY (58232-0750-2) |
| Product NDC | 58232-0750 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride and Zinc Acetate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120322 |
| 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 | 20; 1 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
