{
"NDC": {
"NDCCode": "69352-020-01",
"PackageDescription": "70 mL in 1 CARTON (69352-020-01) ",
"NDC11Code": "69352-0020-01",
"ProductNDC": "69352-020",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Amarte Ultra Veil Ultra Light Sunscreen Fluid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Octinoxate, Titanium Dioxide, Octisalate, Zinc Oxide",
"DosageFormName": "CREAM",
"RouteName": "TOPICAL",
"StartMarketingDate": "20141001",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M020",
"LabelerName": "AMARTEINTERNATIONAL CO., LTD.",
"SubstanceName": "OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE",
"StrengthNumber": "4.9; 3.5; 3.78; 2.1",
"StrengthUnit": "mg/70mL; mg/70mL; mg/70mL; mg/70mL",
"Pharm_Classes": "Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-07-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20141001",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}