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United States · US · US:63736-327_69011005-7548-4563-93a1-bf7e561f6c98
Auro Dri
UNIISPLATC D08AX05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerInsight Pharmaceuticals LLC
CountryUS (United States)
ATC codeD08AX05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11637363271212 BOX in 1 CASE (63736-327-12) / 1 BOTTLE in 1 BOX / 29 mL in 1 BOTTLE
- ndc11637363272424 BOX in 1 CASE (63736-327-24) / 1 BOTTLE in 1 BOX / 29 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
ND2M416302
ISOPROPYL ALCOHOL
RxCUI 797541
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "ND2M416302",
"rxcui": "797541",
"inchikey": "KFZMGEQAYNKOFK-UHFFFAOYSA-N",
"display_name": "ISOPROPYL ALCOHOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "AURICULAR (OTIC)",
"spl_meta": {
"85cb4973-6a81-4d8f-b187-4bf709d93a98": {
"match": "brand_token",
"title": "AURO DRI (ISOPROPYL ALCOHOL) LIQUID [INSIGHT PHARMACEUTICALS LLC]",
"spl_version": "5",
"published_date": "2024-11-05"
}
},
"productid": "63736-327_69011005-7548-4563-93a1-bf7e561f6c98",
"productndc": "63736-327",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ISOPROPYL ALCOHOL",
"proprietary_name": "Auro Dri",
"active_ingred_unit": "mL/100mL",
"application_number": "M014",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Isopropyl alcohol",
"start_marketing_date": "20100614",
"active_numerator_strength": "95"
}Related drugs
Other records sharing ATC code D08AX05.
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