Gentiana Absinthium

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
4895150071
10 AMPULE in 1 BOX (48951-5007-1) / 1 mL in 1 AMPULE

Annotations

UNII (FDA Substance ID)

S72O3284MS

GENTIANA LUTEA ROOT

RxCUI 1307945

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "S72O3284MS",
    "rxcui": "1307945",
    "inchikey": null,
    "display_name": "GENTIANA LUTEA ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1b53081c-717e-46ae-8f86-e6f070c3c97d": {
      "match": "brand_token",
      "title": "GENTIANA ABSINTHIUM LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "3",
      "published_date": "2025-01-09"
    }
  },
  "productid": "48951-5007_2b250370-261d-fe8f-e063-6394a90a6423",
  "productndc": "48951-5007",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GENTIANA LUTEA ROOT; STRYCHNOS NUX-VOMICA SEED; TARAXACUM PALUSTRE ROOT; WORMWOOD",
  "proprietary_name": "Gentiana Absinthium",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Gentiana Absinthium",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "3; 6; 3; 3"
}

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