Aletris farinosa

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
0220016041
30 [hp_C] in 1 TUBE (0220-0160-41)

Annotations

UNII (FDA Substance ID)

O021JGR97X

ALETRIS FARINOSA ROOT

RxCUI 1309950

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "O021JGR97X",
    "rxcui": "1309950",
    "inchikey": null,
    "display_name": "ALETRIS FARINOSA ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "87ae7310-927b-48fe-b659-6f93dad62363": {
      "match": "brand_token",
      "title": "ALETRIS COMBINATION 9203 (ALETRIS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "0220-0160_15eb77f6-1ccd-ba49-e063-6394a90a20e1",
  "productndc": "0220-0160",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALETRIS FARINOSA ROOT",
  "proprietary_name": "Aletris farinosa",
  "active_ingred_unit": "[hp_C]/30[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "ALETRIS FARINOSA ROOT",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

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