Chelidonium comp.

UNIISPL

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

Identification

ManufacturerUriel Pharmacy, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895132813
60 mL in 1 BOTTLE, DROPPER (48951-3281-3)

Annotations

UNII (FDA Substance ID)

FLT36UCF0N

CHELIDONIUM MAJUS ROOT

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "FLT36UCF0N",
    "rxcui": null,
    "inchikey": null,
    "display_name": "CHELIDONIUM MAJUS ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "615401fd-eeca-4aaa-8656-0fc8e4eb7ca3": {
      "match": "brand_token",
      "title": "CHELIDONIUM COMBINATION 9217 (CHELIDONIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "48951-3281_2df4687c-a157-13ac-e063-6294a90aa494",
  "productndc": "48951-3281",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CHELIDONIUM MAJUS ROOT; MILK THISTLE; ONOPORDUM ACANTHIUM FLOWER; PTERIDIUM AQUILINUM WHOLE; SALIX PURPUREA BARK; TARAXACUM PALUSTRE ROOT; URTICA DIOICA",
  "proprietary_name": "Chelidonium comp.",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Chelidonium comp.",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "1; 1; 1; 1; 1; 1; 1"
}

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