Equisetum Silicea

UNIISPL

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

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
4895140393
60 mL in 1 BOTTLE, DROPPER (48951-4039-3)

Annotations

UNII (FDA Substance ID)

1DP6Y6B65Z

EQUISETUM ARVENSE TOP

RxCUI 1306235

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1DP6Y6B65Z",
    "rxcui": "1306235",
    "inchikey": null,
    "display_name": "EQUISETUM ARVENSE TOP",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "e88b820b-4a07-42e2-8fe2-b30729e91a8c": {
      "match": "brand_token",
      "title": "EQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "5",
      "published_date": "2026-03-31"
    }
  },
  "productid": "48951-4039_4e43eb39-76aa-f806-e063-6394a90af572",
  "productndc": "48951-4039",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "EQUISETUM ARVENSE TOP; SILICON DIOXIDE",
  "proprietary_name": "Equisetum Silicea",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Equisetum Silicea",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "3; 3"
}

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