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United States · US · US:65601-759_4b1c1e95-be40-7bb9-e063-6294a90a1757

Ultra Blue Antibacterial Foaming Skin Cleanser

UNIISPLATC D08AJ01

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

Identification

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

Packs · 3

  • ndc11
    6560175904
    3780 mL in 1 BOTTLE (65601-759-04)
  • ndc11
    6560175929
    1000 mL in 1 BAG (65601-759-29)
  • ndc11
    6560175957
    550 mL in 1 BOTTLE, PUMP (65601-759-57)

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": {
    "52d4b1c1-7431-4f8c-e063-6294a90ad482": {
      "match": "brand_token",
      "title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
      "spl_version": "1",
      "published_date": "2026-05-29"
    }
  },
  "productid": "65601-759_4b1c1e95-be40-7bb9-e063-6294a90a1757",
  "productndc": "65601-759",
  "dosage_form": "SOAP",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZALKONIUM CHLORIDE",
  "proprietary_name": "Ultra Blue Antibacterial Foaming Skin Cleanser",
  "active_ingred_unit": "mg/mL",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "benzalkonium chloride",
  "start_marketing_date": "20121112",
  "active_numerator_strength": "1.3"
}

Related drugs

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