Rhus Aconitum

SPL

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
4895181401
10 AMPULE in 1 BOX (48951-8140-1) / 1 mL in 1 AMPULE

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "ORAL",
  "spl_meta": {
    "a176c241-fc2d-4fea-82d9-81183971b4cf": {
      "match": "brand_token",
      "title": "RHUS ACONITUM LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "5",
      "published_date": "2026-03-02"
    }
  },
  "productid": "48951-8140_4bd37192-f7e8-b961-e063-6294a90ab3d3",
  "productndc": "48951-8140",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACONITUM NAPELLUS; ATROPA BELLADONNA; GELSEMIUM SEMPERVIRENS ROOT; MANDRAGORA OFFICINARUM ROOT; PENOXSULAM; PSEUDOGNAPHALIUM LUTEOALBUM LEAF; TOXICODENDRON PUBESCENS LEAF",
  "proprietary_name": "Rhus Aconitum",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Rhus Aconitum",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "6; 6; 4; 6; 10; 4; 6"
}

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