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United States · US · US:52261-0500_d3e2c5a1-5f63-4c96-8fbe-1ba6c8c5d93d

BerbereX Wound Cleanser

UNIISPLATC R02AA

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

Identification

ManufacturerCosco International, Inc.
CountryUS (United States)
ATC codeR02AA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    5226105001
    118 mL in 1 BOTTLE, SPRAY (52261-0500-1)
  • ndc11
    5226105002
    237 mL in 1 BOTTLE, SPRAY (52261-0500-2)
  • ndc11
    5226105003
    473 mL in 1 BOTTLE, SPRAY (52261-0500-3)

Annotations

UNII (FDA Substance ID)
344S277G0Z
ALLANTOIN
RxCUI 508
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "08b28f52-21fc-4694-a163-91c8193b4008": {
      "match": "brand_token",
      "title": "BERBEREX WOUND CLEANSER (BENZETHONIUM CHLORIDE) LIQUID [COSCO INTERNATIONAL, INC.]",
      "spl_version": "7",
      "published_date": "2025-06-02"
    }
  },
  "productid": "52261-0500_d3e2c5a1-5f63-4c96-8fbe-1ba6c8c5d93d",
  "productndc": "52261-0500",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN; BENZETHONIUM CHLORIDE",
  "proprietary_name": "BerbereX Wound Cleanser",
  "active_ingred_unit": "g/1000mL; g/1000mL",
  "application_number": "M003",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Benzethonium Chloride",
  "start_marketing_date": "20150517",
  "active_numerator_strength": "5; 1"
}

Related drugs

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