G-19

UNIISPL

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

Identification

ManufacturerDNA Labs, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5826403822
59.14 mL in 1 BOTTLE, GLASS (58264-0382-2)

Annotations

UNII (FDA Substance ID)

9Z32IEA9F7

ILEX AQUIFOLIUM LEAF

RxCUI 1307755

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "9Z32IEA9F7",
    "rxcui": "1307755",
    "inchikey": null,
    "display_name": "ILEX AQUIFOLIUM LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "411fd7e6-1a91-4d19-b394-c713c88e2130": {
      "match": "brand_token",
      "title": "G-19 (ILEX AQUIFOLIUM LEAF) SOLUTION [DNA LABS, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "58264-0382_2b5342c6-d3bc-693f-e063-6294a90a90e2",
  "productndc": "58264-0382",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ILEX AQUIFOLIUM LEAF",
  "proprietary_name": "G-19",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "ILEX AQUIFOLIUM LEAF",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "1"
}

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