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United States · US · US:21749-610_2a976ebe-2fd0-a496-e063-6294a90a2dae
PURELL Antimicrobial Foaming Hand
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGOJO Industries, Inc.
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1121749610401200 mL in 1 PACKAGE (21749-610-40)
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": {
"52d04540-b14b-8c88-e063-6394a90afd39": {
"match": "brand_token",
"title": "PURELL ADVANCED HAND SANITIZER E3 GEL (ALCOHOL) GEL [GOJO INDUSTRIES, LLC]",
"spl_version": "1",
"published_date": "2026-05-28"
}
},
"productid": "21749-610_2a976ebe-2fd0-a496-e063-6294a90a2dae",
"productndc": "21749-610",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "PURELL Antimicrobial Foaming Hand",
"active_ingred_unit": "mg/100mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzalkonium Chloride",
"start_marketing_date": "20231211",
"active_numerator_strength": ".5"
}Related drugs
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