BERBERIS AQUIFOLIUM

UNIISPL

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

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220085341
200 [kp_C] in 1 TUBE (0220-0853-41)

Annotations

UNII (FDA Substance ID)

VZJ9F3C3SB

BERBERIS AQUIFOLIUM ROOT BARK

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "VZJ9F3C3SB",
    "rxcui": null,
    "inchikey": null,
    "display_name": "BERBERIS AQUIFOLIUM ROOT BARK",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "5da48d70-1140-495d-b672-0e55c04196e1": {
      "match": "brand_token",
      "title": "BERBERIS QUARTZ LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "5",
      "published_date": "2026-01-19"
    }
  },
  "productid": "0220-0853_3b3c96d0-56f1-2278-e063-6394a90a5c36",
  "productndc": "0220-0853",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BERBERIS AQUIFOLIUM ROOT BARK",
  "proprietary_name": "BERBERIS AQUIFOLIUM",
  "active_ingred_unit": "[kp_C]/200[kp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "BERBERIS AQUIFOLIUM ROOT BARK",
  "start_marketing_date": "20250101",
  "active_numerator_strength": "200"
}

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