Thiosinaminum

UNIISPL

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 · 4

ndc11
3766223081
200 PELLET in 1 VIAL, GLASS (37662-2308-1)
ndc11
3766223082
500 PELLET in 1 VIAL, GLASS (37662-2308-2)
ndc11
3766223083
3000 PELLET in 1 BOTTLE, GLASS (37662-2308-3)
ndc11
3766223084
10000 PELLET in 1 BOTTLE, GLASS (37662-2308-4)

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": {
    "09a60d62-a479-0f02-e063-6294a90a6d39": {
      "match": "brand_token",
      "title": "THIOSINAMINUM (ALLYLTHIOUREA) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]",
      "spl_version": "2",
      "published_date": "2025-01-30"
    }
  },
  "productid": "37662-2308_f1f61f7e-bb41-4ee8-e053-2a95a90a08bd",
  "productndc": "37662-2308",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLYLTHIOUREA",
  "proprietary_name": "Thiosinaminum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Thiosinaminum",
  "start_marketing_date": "20230111",
  "active_numerator_strength": "100"
}

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