| NDC Code | 58232-0742-6 |
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| Package Description | 1 APPLICATOR in 1 CARTON (58232-0742-6) / 14 mL in 1 APPLICATOR |
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| Product NDC | 58232-0742 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Benadryl Extra Strength Itch Relief |
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| Non-Proprietary Name | Diphenhydramine Hydrochloride And Zinc Acetate |
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| Dosage Form | SOLUTION |
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| Usage | TOPICAL |
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| Start Marketing Date | 20120401 |
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| End Marketing Date | 20230221 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part347 |
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| Manufacturer | Johnson & Johnson Consumer Inc. |
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| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
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| Strength | 20; 1 |
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| Strength Unit | mg/mL; mg/mL |
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| Pharmacy Classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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