Bismuthum Oxydatum

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
6354548801
200 PELLET in 1 VIAL, GLASS (63545-488-01)
ndc11
6354548802
500 PELLET in 1 VIAL, GLASS (63545-488-02)
ndc11
6354548803
3000 PELLET in 1 BOTTLE, GLASS (63545-488-03)
ndc11
6354548804
10000 PELLET in 1 BOTTLE, GLASS (63545-488-04)

Annotations

UNII (FDA Substance ID)

A6I4E79QF1

BISMUTH OXIDE

RxCUI 19472

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "A6I4E79QF1",
    "rxcui": "19472",
    "inchikey": "TYIXMATWDRGMPF-UHFFFAOYSA-N",
    "display_name": "BISMUTH OXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "39e8a434-071f-b2b0-e063-6294a90acd00": {
      "match": "brand_token",
      "title": "BISMUTHUM SUBNITRICUM (BISMUTH SUBNITRATE) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-19"
    }
  },
  "productid": "63545-488_de0d2bf6-962a-7c7a-e053-2a95a90a1616",
  "productndc": "63545-488",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH OXIDE",
  "proprietary_name": "Bismuthum Oxydatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Bismuthum Oxydatum",
  "start_marketing_date": "20220502",
  "active_numerator_strength": "500"
}

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