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United States · US · US:11084-021_70390f59-9b71-4614-be06-57ae24e8ec5c
Antibacterial Foam
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSC Johnson Professional USA Inc.
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1111084021053.78 L in 1 BOTTLE, PLASTIC (11084-021-05)
- ndc11110840214218.93 L in 1 PAIL (11084-021-42)
- ndc111108402155208.2 L in 1 DRUM (11084-021-55)
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": {
"960bfe55-87f6-3e51-e053-2995a90a867d": {
"match": "brand_token",
"title": "ANTIBACTERIAL LIDOCAINE WOUND GEL (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) GEL [CVS PHARMACY]",
"spl_version": "5",
"published_date": "2026-05-28"
}
},
"productid": "11084-021_70390f59-9b71-4614-be06-57ae24e8ec5c",
"productndc": "11084-021",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "Antibacterial Foam",
"active_ingred_unit": "g/L",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzalkonium Chloride",
"start_marketing_date": "20170801",
"active_numerator_strength": "1.3"
}Related drugs
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