84066-109-01 : NDC 2026 Code

84066-109-01 : Homosalate,octocrylene, Phenylbenzimidazole Sulfonic Acid, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane ( Medultima Adventure Sunscreen )

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NDC Code : 84066-109-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "84066-109-01",
    "PackageDescription": "50 g in 1 BOTTLE (84066-109-01) ",
    "NDC11Code": "84066-0109-01",
    "ProductNDC": "84066-109",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Medultima Adventure Sunscreen",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Homosalate,octocrylene, Phenylbenzimidazole Sulfonic Acid, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane",
    "DosageFormName": "CREAM",
    "RouteName": "TOPICAL",
    "StartMarketingDate": "20260604",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH DRUG",
    "ApplicationNumber": "M020",
    "LabelerName": "Guangzhou Tata Biotechnology Co., Ltd.",
    "SubstanceName": "BUTYL METHOXYDIBENZOYLMETHANE; ETHYLHEXYL SALICYLATE; HOMOSALATE; OCTOCRYLENE; PHENYLBENZIMIDAZOLE SULFONIC ACID",
    "StrengthNumber": "3; 4; 9; 7; 4",
    "StrengthUnit": "g/100g; g/100g; g/100g; g/100g; g/100g",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-06-08",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260604",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}