🇺🇸
United States · US · US:66949-139_46dfe3ae-bb1d-7a50-e063-6394a90a96c7
AFCO 5508 Sanifect Foam-E II
UNIISPLATC D08AE05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZep Inc.
CountryUS (United States)
ATC codeD08AE05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc116694913901208198 mL in 1 DRUM (66949-139-01)
- ndc1166949139026000 mL in 1 CASE (66949-139-02)
- ndc1166949139033785 mL in 1 CASE (66949-139-03)
Annotations
UNII (FDA Substance ID)
0F32U78V2Q
CHLOROXYLENOL
RxCUI 20877
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0F32U78V2Q",
"rxcui": "20877",
"inchikey": "OSDLLIBGSJNGJE-UHFFFAOYSA-N",
"display_name": "CHLOROXYLENOL",
"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": "66949-139_46dfe3ae-bb1d-7a50-e063-6394a90a96c7",
"productndc": "66949-139",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CHLOROXYLENOL",
"proprietary_name": "AFCO 5508 Sanifect Foam-E II",
"active_ingred_unit": "mg/208198mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Ethanol",
"start_marketing_date": "20250505",
"active_numerator_strength": "2081980"
}Related drugs
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