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United States · US · US:58264-0370_2b531912-67dc-6172-e063-6394a90a178f

G-7

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

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
    5826403702
    59.14 mL in 1 BOTTLE, GLASS (58264-0370-2)

Annotations

UNII (FDA Substance ID)
5HW39H9KDH
BETULA PENDULA LEAF
RxCUI 1351786
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5HW39H9KDH",
    "rxcui": "1351786",
    "inchikey": null,
    "display_name": "BETULA PENDULA LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "4f45aef4-def2-4464-9a17-19db9cb64985": {
      "match": "brand_token",
      "title": "G-7 (BETULA PUBESCENS FLOWER BUD AND BETULA PENDULA LEAF) SOLUTION [DNA LABS, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "58264-0370_2b531912-67dc-6172-e063-6394a90a178f",
  "productndc": "58264-0370",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BETULA PENDULA LEAF; BETULA PUBESCENS FLOWER BUD",
  "proprietary_name": "G-7",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "BETULA PUBESCENS FLOWER BUD and BETULA PENDULA LEAF",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "1; 1"
}

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