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United States · US · US:63545-080_bc1c6150-aa63-f9b1-e053-2995a90a07d0

Aralia Racemosa

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerHahnemann Laboratories, Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    6354508001
    200 PELLET in 1 VIAL, GLASS (63545-080-01)
  • ndc11
    6354508002
    1200 PELLET in 1 BOTTLE, GLASS (63545-080-02)
  • ndc11
    6354508003
    4000 PELLET in 1 BOTTLE, GLASS (63545-080-03)

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": "63545-080_bc1c6150-aa63-f9b1-e053-2995a90a07d0",
  "productndc": "63545-080",
  "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": "6"
}

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