Xanthoxylum Fraxineum

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766224061
80 PELLET in 1 VIAL, GLASS (37662-2406-1)
ndc11
3766224062
200 PELLET in 1 VIAL, GLASS (37662-2406-2)
ndc11
3766224063
1200 PELLET in 1 BOTTLE, GLASS (37662-2406-3)
ndc11
3766224064
4000 PELLET in 1 BOTTLE, GLASS (37662-2406-4)

Annotations

UNII (FDA Substance ID)

A4KL1HMZ7T

ZANTHOXYLUM AMERICANUM BARK

RxCUI 1310155

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "A4KL1HMZ7T",
    "rxcui": "1310155",
    "inchikey": null,
    "display_name": "ZANTHOXYLUM AMERICANUM BARK",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3a0db5f6-4fa5-23bb-e063-6294a90abdf5": {
      "match": "brand_token",
      "title": "XANTHOXYLUM FRAXINEUM (ZANTHOXYLUM AMERICANUM BARK) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-21"
    }
  },
  "productid": "37662-2406_f2946bb3-57bc-216b-e053-2995a90ab015",
  "productndc": "37662-2406",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZANTHOXYLUM AMERICANUM BARK",
  "proprietary_name": "Xanthoxylum Fraxineum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Xanthoxylum Fraxineum",
  "start_marketing_date": "20230118",
  "active_numerator_strength": "30"
}

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