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United States · US · US:83986-118_4cc3d5ce-f601-93a5-e063-6294a90a7296
Foaming Hand Sanitizer
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUpLift Brands LLC
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1183986118451150 mL in 1 BOTTLE, PLASTIC (83986-118-45)
- ndc1183986118861000 mL in 1 BOTTLE, PLASTIC (83986-118-86)
- ndc118398611896221 mL in 1 BOTTLE, PLASTIC (83986-118-96)
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": "83986-118_4cc3d5ce-f601-93a5-e063-6294a90a7296",
"productndc": "83986-118",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "Foaming Hand Sanitizer",
"active_ingred_unit": "mg/mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzalkonium Chloride",
"start_marketing_date": "20240229",
"active_numerator_strength": "1.3"
}Related drugs
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