| NDC Code | 47682-865-29 |
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| Package Description | 35.4 TUBE in 1 BOX (47682-865-29) / 35 g in 1 TUBE |
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| Product NDC | 47682-865 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Medi First Extra Strength Itch Relief |
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| Non-Proprietary Name | Diphenhydramine, Zinc Acetate |
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| Dosage Form | CREAM |
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| Usage | TOPICAL |
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| Start Marketing Date | 20251101 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M017 |
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| Manufacturer | Unifirst First Aid Corporation |
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| Substance Name | ZINC ACETATE; DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | .2; .001 |
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| Strength Unit | g/g; g/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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