πΊπΈ
United States Β· US Β· US:15631-2868_1a223bf8-fc34-dbcd-e063-6394a90a263e
NUX VOMICA
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 2
- ndc11156312868010 mL in 1 BOTTLE (15631-2868-0)
- ndc11156312868130 mL in 1 BOTTLE (15631-2868-1)
Annotations
UNII (FDA Substance ID)
269XH13919
STRYCHNOS NUX-VOMICA SEED
RxCUI 1309678
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "269XH13919",
"rxcui": "1309678",
"inchikey": null,
"display_name": "STRYCHNOS NUX-VOMICA SEED",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"28f6663d-0a00-4650-a84e-b625024687d3": {
"match": "brand_token",
"title": "NUX VOMICA COMBINATION 9235 (NUX VOMICA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
"spl_version": "2",
"published_date": "2026-01-12"
}
},
"productid": "15631-2868_1a223bf8-fc34-dbcd-e063-6394a90a263e",
"productndc": "15631-2868",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "STRYCHNOS NUX-VOMICA SEED",
"proprietary_name": "NUX VOMICA",
"active_ingred_unit": "[hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "NUX VOMICA",
"start_marketing_date": "20240523",
"active_numerator_strength": "3"
}Access this data programmatically
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