Thiosinominum

UNIISPL

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

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220499041
6 [hp_X] in 1 TUBE (0220-4990-41)

Annotations

UNII (FDA Substance ID)

706IDJ14B7

ALLYLTHIOUREA

RxCUI 1318494

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "706IDJ14B7",
    "rxcui": "1318494",
    "inchikey": "HTKFORQRBXIQHD-UHFFFAOYSA-N",
    "display_name": "ALLYLTHIOUREA",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "8773567e-26ba-0ed6-e053-2995a90aff91": {
      "match": "brand_token",
      "title": "THIOSINOMINUM (ALLYLTHIOUREA\t) PELLET [BOIRON]",
      "spl_version": "2",
      "published_date": "2023-11-16"
    }
  },
  "productid": "0220-4990_0a349bfa-bb8a-ddb1-e063-6294a90a5772",
  "productndc": "0220-4990",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLYLTHIOUREA",
  "proprietary_name": "Thiosinominum",
  "active_ingred_unit": "[hp_X]/6[hp_X]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "ALLYLTHIOUREA",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "6"
}

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