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United States · US · US:68306-109_4c3916d9-06d1-db22-e063-6394a90aee43
Avant Foaming Hand Sanitizer
UNIISPLATC D08AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerB4 Soap LLC
CountryUS (United States)
ATC codeD08AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc116830610901530 mL in 1 BOTTLE, PUMP (68306-109-01)
- ndc1168306109021000 mL in 1 POUCH (68306-109-02)
- ndc1168306109031000 mL in 1 CARTRIDGE (68306-109-03)
- ndc1168306109051040988 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (68306-109-05)
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": {
"241f4334-2e88-4f7b-a0c7-c93da9f5086c": {
"match": "brand_token",
"title": "AVANT 70% ALCOHOL GEL (ALCOHOL) GEL [B4 SOAP LLC]",
"spl_version": "3",
"published_date": "2026-03-20"
}
},
"productid": "68306-109_4c3916d9-06d1-db22-e063-6394a90aee43",
"productndc": "68306-109",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALCOHOL",
"proprietary_name": "Avant Foaming Hand Sanitizer",
"active_ingred_unit": "mL/100mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Alcohol",
"start_marketing_date": "20101208",
"active_numerator_strength": "62"
}Related drugs
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