Ceanothus americanus

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
0220123141
30 [hp_C] in 1 TUBE (0220-1231-41)

Annotations

UNII (FDA Substance ID)

25B1Y14T8N

CEANOTHUS AMERICANUS LEAF

RxCUI 1309757

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "25B1Y14T8N",
    "rxcui": "1309757",
    "inchikey": null,
    "display_name": "CEANOTHUS AMERICANUS LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "76007366-ba3c-4c7b-9dab-69306aedd57c": {
      "match": "brand_token",
      "title": "CEANOTHUS COMBINATION 9216 (CEANOTHUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "0220-1231_09bef660-9f66-48d2-e063-6394a90a2104",
  "productndc": "0220-1231",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CEANOTHUS AMERICANUS LEAF",
  "proprietary_name": "Ceanothus americanus",
  "active_ingred_unit": "[hp_C]/30[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "CEANOTHUS AMERICANUS LEAF",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

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