🇺🇸
United States · US · US:59900-125_288cba7a-1f65-6d80-e063-6394a90aca47
ALPET E3 HAND SANITIZER FOAM
UNIISPLATC D08AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBest Sanitizers, Inc.
CountryUS (United States)
ATC codeD08AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc115990012502208197 mL in 1 DRUM (59900-125-02)
- ndc1159900125033785 mL in 1 JUG (59900-125-03)
- ndc1159900125051250 mL in 1 BOTTLE (59900-125-05)
- ndc115990012508250 mL in 1 BOTTLE (59900-125-08)
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": {
"0aa71f9d-f660-4a32-b54a-1968aea9d0ee": {
"match": "brand_token",
"title": "ALPET QE2 SANITIZING FOAM (BENZALKONIUM CHLORIDE) LIQUID [BEST SANITIZERS, INC.]",
"spl_version": "2",
"published_date": "2024-12-23"
}
},
"productid": "59900-125_288cba7a-1f65-6d80-e063-6394a90aca47",
"productndc": "59900-125",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALCOHOL",
"proprietary_name": "ALPET E3 HAND SANITIZER FOAM",
"active_ingred_unit": "mL/100mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "ALCOHOL",
"start_marketing_date": "20190501",
"active_numerator_strength": "62"
}Related drugs
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