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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

  • ndc11
    4895172142
    30 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"
}

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