{
"NDC": {
"NDCCode": "68726-265-37",
"PackageDescription": "7.4 mL in 1 TUBE (68726-265-37) ",
"NDC11Code": "68726-0265-37",
"ProductNDC": "68726-265",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Daily Defense",
"ProprietaryNameSuffix": "Spf 50",
"NonProprietaryName": "Face Sunscreen",
"DosageFormName": "LOTION",
"RouteName": "TOPICAL",
"StartMarketingDate": "20200501",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M020",
"LabelerName": "CP Skin Health Group, Inc.",
"SubstanceName": "OCTISALATE; OCTOCRYLENE; ZINC OXIDE",
"StrengthNumber": "5; 10; 9.1",
"StrengthUnit": "g/100mL; g/100mL; g/100mL",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-10-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20200501",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}