UNDA 700

UNII

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

Identification

ManufacturerSeroyal USA

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6210611718
1 BOTTLE, GLASS in 1 CARTON (62106-1171-8) / 20 mL in 1 BOTTLE, GLASS

Annotations

UNII (FDA Substance ID)

1TH8Q20J0U

BERBERIS VULGARIS ROOT BARK

RxCUI 1309766

Raw payload (JSON)

{
  "unii": {
    "unii": "1TH8Q20J0U",
    "rxcui": "1309766",
    "inchikey": null,
    "display_name": "BERBERIS VULGARIS ROOT BARK",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "62106-1171_c733ec78-5b43-7a7c-e053-2995a90a2f9a",
  "productndc": "62106-1171",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BERBERIS VULGARIS ROOT BARK; CALCIUM FLUORIDE",
  "proprietary_name": "UNDA 700",
  "active_ingred_unit": "[hp_X]/20mL; [hp_X]/20mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Berberis vulgaris, Calcarea fluorica",
  "start_marketing_date": "20150923",
  "active_numerator_strength": "4; 12"
}

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