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United States · US · US:51393-7656_c5752aa4-40c2-4f35-a13f-d5684ec08969
Gout
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerForces of Nature
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11513937656111 mL in 1 BOTTLE, DISPENSING (51393-7656-1)
- ndc11513937656330 mL in 1 BOTTLE, DISPENSING (51393-7656-3)
- ndc1151393765644 mL in 1 BOTTLE, DISPENSING (51393-7656-4)
Annotations
UNII (FDA Substance ID)
O80TY208ZW
ARNICA MONTANA WHOLE
RxCUI 285208
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "O80TY208ZW",
"rxcui": "285208",
"inchikey": null,
"display_name": "ARNICA MONTANA WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"41dc03fc-169b-4691-bd62-9a41d7a6d2f7": {
"match": "brand_token",
"title": "GOUT SYMPTOM RELIEF (AMMON PHOS, BELLADONNA, COLCHICUM AUTUMNALE, FORMICUM ACIDUM, FRAXINUS EXCELSIOR, LEDUM PALUSTRE, NATRUM CARBONICUM, NUX VOMICA AND URTICA URENS.) LIQUID [KING BIO INC.]",
"spl_version": "1",
"published_date": "2026-03-10"
}
},
"productid": "51393-7656_c5752aa4-40c2-4f35-a13f-d5684ec08969",
"productndc": "51393-7656",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ARNICA MONTANA WHOLE; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAF; URTICA URENS WHOLE",
"proprietary_name": "Gout",
"active_ingred_unit": "[hp_C]/1000mL; [hp_X]/1000mL; [hp_X]/1000mL; [hp_C]/1000mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Leaf",
"start_marketing_date": "20170215",
"active_numerator_strength": "30; 8; 12; 30"
}Access this data programmatically
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