Scandium Oxydatum

UNII

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
3766229961
10000 PELLET in 1 BOTTLE, GLASS (37662-2996-1)

Annotations

UNII (FDA Substance ID)

T0G94L07ZD

SCANDIUM OXIDE

Raw payload (JSON)

{
  "unii": {
    "unii": "T0G94L07ZD",
    "rxcui": null,
    "inchikey": "HJGMWXTVGKLUAQ-UHFFFAOYSA-N",
    "display_name": "SCANDIUM OXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "37662-2996_f9d0b7ba-bf4d-fe21-e053-6394a90a0621",
  "productndc": "37662-2996",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SCANDIUM OXIDE",
  "proprietary_name": "Scandium Oxydatum",
  "active_ingred_unit": "[hp_Q]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Scandium Oxydatum",
  "start_marketing_date": "20230420",
  "active_numerator_strength": "1"
}

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