Aralia Racemosa

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
6354508501
200 PELLET in 1 VIAL, GLASS (63545-085-01)
ndc11
6354508502
500 PELLET in 1 VIAL, GLASS (63545-085-02)
ndc11
6354508503
3000 PELLET in 1 BOTTLE, GLASS (63545-085-03)
ndc11
6354508504
10000 PELLET in 1 BOTTLE, GLASS (63545-085-04)

Annotations

UNII (FDA Substance ID)

T90W4582DU

ARALIA RACEMOSA ROOT

RxCUI 1309833

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "T90W4582DU",
    "rxcui": "1309833",
    "inchikey": null,
    "display_name": "ARALIA RACEMOSA ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "c7248bb6-187d-4076-85dd-94753f7da3b5": {
      "match": "brand_token",
      "title": "ARALIA COMBINATION 9256 (ARALIA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "63545-085_bc1c6150-aa63-f9b1-e053-2995a90a07d0",
  "productndc": "63545-085",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ARALIA RACEMOSA ROOT",
  "proprietary_name": "Aralia Racemosa",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aralia Racemosa",
  "start_marketing_date": "20210224",
  "active_numerator_strength": "500"
}

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