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United States · US · US:63545-084_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 · 4
- ndc116354508401200 PELLET in 1 VIAL, GLASS (63545-084-01)
- ndc116354508402500 PELLET in 1 VIAL, GLASS (63545-084-02)
- ndc1163545084033000 PELLET in 1 BOTTLE, GLASS (63545-084-03)
- ndc11635450840410000 PELLET in 1 BOTTLE, GLASS (63545-084-04)
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": "63545-084_bc1c6150-aa63-f9b1-e053-2995a90a07d0",
"productndc": "63545-084",
"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": "200"
}Access this data programmatically
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