GUNA-IL 4

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerGuna spa

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1708938218
1 BOTTLE, DROPPER in 1 BOX (17089-382-18) / 30 mL in 1 BOTTLE, DROPPER

Annotations

UNII (FDA Substance ID)

751635Z921

BINETRAKIN

RxCUI 1426682

Raw payload (JSON)

{
  "unii": {
    "unii": "751635Z921",
    "rxcui": "1426682",
    "inchikey": null,
    "display_name": "BINETRAKIN",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "17089-382_ed819152-2968-22be-e053-2a95a90a33f6",
  "productndc": "17089-382",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BINETRAKIN",
  "proprietary_name": "GUNA-IL 4",
  "active_ingred_unit": "[hp_C]/30mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "BINETRAKIN",
  "start_marketing_date": "20080617",
  "active_numerator_strength": "4"
}

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