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United States · US · US:48951-7214_2c907346-28ec-f243-e063-6294a90ae572
Oxalis 1X
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUriel Pharmacy, Inc
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11489517214230 g in 1 TUBE (48951-7214-2)
Annotations
UNII (FDA Substance ID)
3STW243384
OXALIS STRICTA WHOLE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3STW243384",
"rxcui": null,
"inchikey": null,
"display_name": "OXALIS STRICTA WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"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": "48951-7214_2c907346-28ec-f243-e063-6294a90ae572",
"productndc": "48951-7214",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OXALIS STRICTA WHOLE",
"proprietary_name": "Oxalis 1X",
"active_ingred_unit": "[hp_X]/g",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Oxalis 1X",
"start_marketing_date": "20090901",
"active_numerator_strength": "1"
}Access this data programmatically
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