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United States · US · US:51048-005_97808d57-7db1-4ac9-92dd-042eb329dd24
DOP Isopropyl Rubbing Alcohol 70%
UNIISPLATC D08AX05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOmega & Delta Co., Inc.
CountryUS (United States)
ATC codeD08AX05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc115104800504118 mL in 1 BOTTLE, SPRAY (51048-005-04)
- ndc115104800516473 mL in 1 BOTTLE, PLASTIC (51048-005-16)
- ndc115104800532946 mL in 1 BOTTLE, PLASTIC (51048-005-32)
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": "TOPICAL",
"spl_meta": {
"c779a35b-1118-4560-8d77-6878edb4c267": {
"match": "brand_token",
"title": "DOP ISOPROPYL RUBBING ALCOHOL 70% (ISOPROPYL ALCOHOL) LIQUID [OMEGA & DELTA CO., INC.]",
"spl_version": "4",
"published_date": "2026-01-28"
}
},
"productid": "51048-005_97808d57-7db1-4ac9-92dd-042eb329dd24",
"productndc": "51048-005",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ISOPROPYL ALCOHOL",
"proprietary_name": "DOP Isopropyl Rubbing Alcohol 70%",
"active_ingred_unit": "mL/100mL",
"application_number": "M003",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "ISOPROPYL ALCOHOL",
"start_marketing_date": "20000101",
"active_numerator_strength": "70"
}Related drugs
Other records sharing ATC code D08AX05.
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