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United States · US · US:67777-403_4db3b7d3-81f1-d779-e063-6394a90a83df

DURMA DynaWound Cleanser

UNIISPLATC D08AJ08

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

Identification

ManufacturerDynarex Corporation
CountryUS (United States)
ATC codeD08AJ08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    6777740302
    24 BOTTLE, SPRAY in 1 CASE (67777-403-02) / 236.5 mL in 1 BOTTLE, SPRAY (67777-403-01)
  • ndc11
    6777740304
    12 BOTTLE in 1 CASE (67777-403-04) / 118.3 mL in 1 BOTTLE (67777-403-03)

Annotations

UNII (FDA Substance ID)
PH41D05744
BENZETHONIUM CHLORIDE
RxCUI 40036
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "PH41D05744",
    "rxcui": "40036",
    "inchikey": "UREZNYTWGJKWBI-UHFFFAOYSA-M",
    "display_name": "BENZETHONIUM CHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "6a4dd82a-6b06-426b-9afd-415a1a4339b4": {
      "match": "brand_token",
      "title": "DURMA DYNAWOUND CLEANSER (WOUND CLEANSER) SPRAY [DYNAREX CORPORATION]",
      "spl_version": "8",
      "published_date": "2026-03-24"
    }
  },
  "productid": "67777-403_4db3b7d3-81f1-d779-e063-6394a90a83df",
  "productndc": "67777-403",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZETHONIUM CHLORIDE",
  "proprietary_name": "DURMA DynaWound Cleanser",
  "active_ingred_unit": "g/100mL",
  "application_number": "M003",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Wound Cleanser",
  "start_marketing_date": "20170213",
  "active_numerator_strength": ".13"
}

Related drugs

Other records sharing ATC code D08AJ08.

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