| NDC Code | 51672-2089-2 |
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| Package Description | 1 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE |
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| Product NDC | 51672-2089 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Diphenhydramine Hydrochloride And Zinc Acetate |
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| Non-Proprietary Name | Diphenhydramine Hydrochloride And Zinc Acetate |
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| Dosage Form | CREAM |
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| Usage | TOPICAL |
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| Start Marketing Date | 20050920 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M017 |
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| Manufacturer | Sun Pharmaceutical Industries, 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/g; mg/g |
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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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