G-41

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
5826404042
59.14 mL in 1 BOTTLE, GLASS (58264-0404-2)

Annotations

UNII (FDA Substance ID)

I2AHJ0JD5V

ULMUS GLABRA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "I2AHJ0JD5V",
    "rxcui": null,
    "inchikey": null,
    "display_name": "ULMUS GLABRA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "9dc69a72-b1ac-4401-8c38-ccc9d775fdfc": {
      "match": "brand_token",
      "title": "G-41 (ULMUS GLABRA WHOLE) SOLUTION [DNA LABS, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "58264-0404_2b533c4d-d42d-4cac-e063-6294a90a7d51",
  "productndc": "58264-0404",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ULMUS GLABRA WHOLE",
  "proprietary_name": "G-41",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "ULMUS GLABRA WHOLE",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "1"
}

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