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United States · US · US:11344-224_4cd559bd-73d9-fdfb-e063-6294a90a0afe
Foaming Hand
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNice-Pak Products, LLC
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1111344224083785 mL in 1 BOTTLE, PLASTIC (11344-224-08)
- ndc1111344224451150 mL in 1 BOTTLE, PLASTIC (11344-224-45)
- ndc1111344224861000 mL in 1 BOTTLE, DISPENSING (11344-224-86)
Annotations
UNII (FDA Substance ID)
F5UM2KM3W7
BENZALKONIUM CHLORIDE
RxCUI 1379
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F5UM2KM3W7",
"rxcui": "1379",
"inchikey": null,
"display_name": "BENZALKONIUM CHLORIDE",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"b2e22e51-88f5-4391-8705-3855c1645d80": {
"match": "brand_token",
"title": "FOAMING SANITIZING HAND (ALCOHOL) SOAP [KUTOL PRODUCTS COMPANY]",
"spl_version": "9",
"published_date": "2026-04-27"
}
},
"productid": "11344-224_4cd559bd-73d9-fdfb-e063-6294a90a0afe",
"productndc": "11344-224",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "Foaming Hand",
"active_ingred_unit": "mg/mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzalkonium Chloride",
"start_marketing_date": "20180208",
"active_numerator_strength": "1.3"
}Related drugs
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