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United States · US · US:53645-1950_fd277f13-f1e8-033d-e053-6294a90a0250
Oxalis Montana 6X
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTrue Botanica, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11536451950223 g in 1 BOTTLE (53645-1950-2)
Annotations
UNII (FDA Substance ID)
GON5VU1D0Z
OXALIS ACETOSELLA WHOLE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "GON5VU1D0Z",
"rxcui": null,
"inchikey": null,
"display_name": "OXALIS ACETOSELLA WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"49de8ed6-b5e8-e8ea-e063-6394a90ad071": {
"match": "brand_token",
"title": "OXALIS 5X OINTMENT [URIEL PHARMACY, INC]",
"spl_version": "1",
"published_date": "2026-02-04"
}
},
"productid": "53645-1950_fd277f13-f1e8-033d-e053-6294a90a0250",
"productndc": "53645-1950",
"dosage_form": "GLOBULE",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OXALIS ACETOSELLA WHOLE",
"proprietary_name": "Oxalis Montana 6X",
"active_ingred_unit": "[hp_X]/23g",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Oxalis Montana 6X",
"start_marketing_date": "20230602",
"active_numerator_strength": "6"
}Access this data programmatically
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