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United States · US · US:68041-512_217f951b-d438-4d3e-aa24-4b820926caa1

Foaming Antibacterial Handsoap

UNIISPLATC D08AJ01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerChemcor Chemical Corporation
CountryUS (United States)
ATC codeD08AJ01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    6804151201
    3780 mL in 1 BOTTLE (68041-512-01)
  • ndc11
    6804151255
    207900 mL in 1 DRUM (68041-512-55)

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": {
    "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": "68041-512_217f951b-d438-4d3e-aa24-4b820926caa1",
  "productndc": "68041-512",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZALKONIUM CHLORIDE",
  "proprietary_name": "Foaming Antibacterial Handsoap",
  "active_ingred_unit": "mg/mL",
  "application_number": "M",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Benzalkonium chloride",
  "start_marketing_date": "20200715",
  "active_numerator_strength": ".0013"
}

Related drugs

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