{
"NDC": {
"NDCCode": "63083-2084-2",
"PackageDescription": "59 mL in 1 BOTTLE, DROPPER (63083-2084-2) ",
"NDC11Code": "63083-2084-02",
"ProductNDC": "63083-2084",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Anti-scar Drops",
"ProprietaryNameSuffix": "2084",
"NonProprietaryName": "Anti-scar Drops",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "19840815",
"EndMarketingDate": null,
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"ApplicationNumber": null,
"LabelerName": "Professional Complementary Health Formulas",
"SubstanceName": "ACONITUM NAPELLUS WHOLE; ALLYLTHIOUREA; ANHYDROUS DIBASIC CALCIUM PHOSPHATE; ARNICA MONTANA WHOLE; GRAPHITE; LACTOSE, X-RAY EXPOSED (1000 RAD); NITRIC ACID; POTASSIUM ALUM; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAF",
"StrengthNumber": "6; 6; 6; 100; 12; 60; 8; 6; 6; 3",
"StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-01-13",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "19850815",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}