Oxalis 20%

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerUriel Pharmcy, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895172215
60 g in 1 TUBE (48951-7221-5)

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": "48951-7221_3b52ff8d-4b88-d598-e063-6294a90aebd0",
  "productndc": "48951-7221",
  "dosage_form": "OINTMENT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OXALIS STRICTA WHOLE",
  "proprietary_name": "Oxalis 20%",
  "active_ingred_unit": "[hp_X]/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Oxalis 20%",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "1"
}

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