47682-865-29 : NDC 2026 Code

47682-865-29 : Diphenhydramine, Zinc Acetate ( Medi First Extra Strength Itch Relief )

Additionally :

You can get information about “47682-865-29” NDC code in 47682-865-29 in HTML format

HTML | 47682-865-29 in TXT (Plain Text) format

TXT | 47682-865-29 in PDF (Portable Document Format)

PDF | 47682-865-29 in XML format

XML formats.

NDC Code : 47682-865-29 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "47682-865-29",
    "PackageDescription": "35.4 TUBE in 1 BOX (47682-865-29)  / 35 g in 1 TUBE",
    "NDC11Code": "47682-0865-29",
    "ProductNDC": "47682-865",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Medi First Extra Strength Itch Relief",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diphenhydramine, Zinc Acetate",
    "DosageFormName": "CREAM",
    "RouteName": "TOPICAL",
    "StartMarketingDate": "20251101",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH DRUG",
    "ApplicationNumber": "M017",
    "LabelerName": "Unifirst First Aid Corporation",
    "SubstanceName": "DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE",
    "StrengthNumber": ".2; .001",
    "StrengthUnit": "g/g; g/g",
    "Pharm_Classes": "Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-06-18",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20251101",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}