GUNA-EGF

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
1708937218
1 BOTTLE, DROPPER in 1 BOX (17089-372-18) / 30 mL in 1 BOTTLE, DROPPER

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Raw payload (JSON)

{
  "route": "ORAL",
  "productid": "17089-372_82de46fa-983c-fade-e053-2991aa0aea95",
  "productndc": "17089-372",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HUMAN EPIDERMAL GROWTH FACTOR",
  "proprietary_name": "GUNA-EGF",
  "active_ingred_unit": "[hp_C]/30mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "EPIDERMAL GROWTH FACTOR",
  "start_marketing_date": "20110331",
  "active_numerator_strength": "4"
}

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