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United States · US · US:66949-140_46dec692-429e-3b0f-e063-6394a90ad672
AFCO 5511 Sanifect E3
UNIISPLATC D08AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZep Inc.
CountryUS (United States)
ATC codeD08AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc116694914001208198 mL in 1 DRUM (66949-140-01)
- ndc1166949140026000 mL in 1 CASE (66949-140-02)
- ndc1166949140033785 mL in 1 CASE (66949-140-03)
Annotations
UNII (FDA Substance ID)
3K9958V90M
ALCOHOL
RxCUI 448
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3K9958V90M",
"rxcui": "448",
"inchikey": "LFQSCWFLJHTTHZ-UHFFFAOYSA-N",
"display_name": "ALCOHOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"347995ef-38bd-7cdb-e063-6394a90adec3": {
"match": "brand_token",
"title": "AFCO 5508 SANIFECT FOAM-E II (ETHANOL) LIQUID [ZEP INC.]",
"spl_version": "2",
"published_date": "2025-12-29"
}
},
"productid": "66949-140_46dec692-429e-3b0f-e063-6394a90ad672",
"productndc": "66949-140",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALCOHOL",
"proprietary_name": "AFCO 5511 Sanifect E3",
"active_ingred_unit": "mL/100mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Ethanol",
"start_marketing_date": "20250505",
"active_numerator_strength": "70"
}Related drugs
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