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United States · US · US:55681-041_3dfec50e-44e8-9395-e063-6394a90ae44b
ProCure Antimicrobial Hand
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTwin Med LLC
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1155681041101000 mL in 1 BAG (55681-041-10)
- ndc115568104175222 mL in 1 BOTTLE, PUMP (55681-041-75)
- ndc115568104180800 mL in 1 BAG (55681-041-80)
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": {
"3d848ec8-5197-6d39-e063-6394a90aaef6": {
"match": "brand_token",
"title": "PROCURE FOAMING HAND SANITIZER (ETHYL ALCOHOL 72%) GEL [TWIN MED LLC]",
"spl_version": "2",
"published_date": "2026-06-01"
}
},
"productid": "55681-041_3dfec50e-44e8-9395-e063-6394a90ae44b",
"productndc": "55681-041",
"dosage_form": "SOAP",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "ProCure Antimicrobial Hand",
"active_ingred_unit": "g/100mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Hand Soap Benzalkonium Chloride (0.13%)",
"start_marketing_date": "20250904",
"active_numerator_strength": ".13"
}Related drugs
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Access this data programmatically
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