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United States · US · US:50865-213_298e23fa-a68d-383f-e063-6294a90a2e34

Foaming Advanced Antibacterial Hand

UNIISPLATC D08AJ01

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

Identification

ManufacturerKutol Products Company
CountryUS (United States)
ATC codeD08AJ01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    5086521313
    3785 mL in 1 BOTTLE, PLASTIC (50865-213-13)
  • ndc11
    5086521317
    50 mL in 1 BOTTLE, PLASTIC (50865-213-17)
  • ndc11
    5086521341
    1000 mL in 1 BAG (50865-213-41)
  • ndc11
    5086521350
    1200 mL in 1 BAG (50865-213-50)
  • ndc11
    5086521352
    1000 mL in 1 BOTTLE, PLASTIC (50865-213-52)
  • ndc11
    5086521378
    950 mL in 1 BOTTLE, PLASTIC (50865-213-78)

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": "50865-213_298e23fa-a68d-383f-e063-6294a90a2e34",
  "productndc": "50865-213",
  "dosage_form": "SOAP",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZALKONIUM CHLORIDE",
  "proprietary_name": "Foaming Advanced Antibacterial Hand",
  "active_ingred_unit": "mg/mL",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "benzalkonium chloride",
  "start_marketing_date": "20151001",
  "active_numerator_strength": ".003"
}

Related drugs

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