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United States · US · US:37662-1939_ed7dc116-4d60-e101-e053-2995a90a545d
Rheum Officinale
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
- ndc11376621939180 PELLET in 1 VIAL, GLASS (37662-1939-1)
- ndc113766219392200 PELLET in 1 VIAL, GLASS (37662-1939-2)
- ndc1137662193931200 PELLET in 1 BOTTLE, GLASS (37662-1939-3)
- ndc1137662193944000 PELLET in 1 BOTTLE, GLASS (37662-1939-4)
Annotations
UNII (FDA Substance ID)
A47JP5ZG9M
RHEUM OFFICINALE ROOT
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "A47JP5ZG9M",
"rxcui": null,
"inchikey": null,
"display_name": "RHEUM OFFICINALE ROOT",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"f65a41b7-5931-4c62-89a3-7b255757527f": {
"match": "brand_token",
"title": "RHEUM COMBINATION 9240 (RHEUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
"spl_version": "2",
"published_date": "2026-01-12"
}
},
"productid": "37662-1939_ed7dc116-4d60-e101-e053-2995a90a545d",
"productndc": "37662-1939",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "RHEUM OFFICINALE ROOT",
"proprietary_name": "Rheum Officinale",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Rheum Officinale",
"start_marketing_date": "20221115",
"active_numerator_strength": "30"
}Access this data programmatically
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