GUNA-IL 12

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
1708939018
1 BOTTLE, DROPPER in 1 BOX (17089-390-18) / 30 mL in 1 BOTTLE, DROPPER

Annotations

UNII (FDA Substance ID)

02FXP10O2U

INTERLEUKIN-12 HUMAN RECOMBINANT

RxCUI 1328172

Raw payload (JSON)

{
  "unii": {
    "unii": "02FXP10O2U",
    "rxcui": "1328172",
    "inchikey": null,
    "display_name": "INTERLEUKIN-12 HUMAN RECOMBINANT",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "17089-390_ed81a1dd-c092-49a5-e053-2995a90aad04",
  "productndc": "17089-390",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "INTERLEUKIN-12 HUMAN RECOMBINANT",
  "proprietary_name": "GUNA-IL 12",
  "active_ingred_unit": "[hp_C]/30mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "INTERLEUKIN-12 HUMAN RECOMBINANT",
  "start_marketing_date": "20080617",
  "active_numerator_strength": "4"
}

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