Aurum 21X

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
4895113181
10 AMPULE in 1 BOX (48951-1318-1) / 1 mL in 1 AMPULE

Annotations

UNII (FDA Substance ID)

79Y1949PYO

GOLD

RxCUI 1311190

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "79Y1949PYO",
    "rxcui": "1311190",
    "inchikey": "PCHJSUWPFVWCPO-UHFFFAOYSA-N",
    "display_name": "GOLD",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "ac80a5ca-01ec-4a16-9f94-eb65f5f2087d": {
      "match": "brand_token",
      "title": "AURUM OLIBANUM MYRRHA LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "4",
      "published_date": "2026-02-27"
    }
  },
  "productid": "48951-1318_48889afd-554b-a47f-e063-6394a90a9bb0",
  "productndc": "48951-1318",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GOLD",
  "proprietary_name": "Aurum 21X",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aurum 21X",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "21"
}

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