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United States · US · US:47593-692_3edaece0-b4c4-46fe-bbbe-fca72128eafd
EXP Foaming Hand Sanitizer
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEcolab Inc.
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1147593692701200 mL in 1 BOTTLE, PLASTIC (47593-692-70)
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": {
"468acf2d-97ff-4cac-91b1-067a1ea382f3": {
"match": "brand_token",
"title": "EXP FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [ECOLAB INC.]",
"spl_version": "1",
"published_date": "2026-01-01"
}
},
"productid": "47593-692_3edaece0-b4c4-46fe-bbbe-fca72128eafd",
"productndc": "47593-692",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "EXP Foaming Hand Sanitizer",
"active_ingred_unit": "mg/100mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzalkonium chloride",
"start_marketing_date": "20251230",
"active_numerator_strength": ".1"
}Related drugs
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