Bismuthum Phosphoricum

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
3766200191
200 PELLET in 1 VIAL, GLASS (37662-0019-1)
ndc11
3766200192
500 PELLET in 1 VIAL, GLASS (37662-0019-2)
ndc11
3766200193
3000 PELLET in 1 BOTTLE, GLASS (37662-0019-3)
ndc11
3766200194
10000 PELLET in 1 BOTTLE, GLASS (37662-0019-4)

Annotations

UNII (FDA Substance ID)

Z9P58L0522

BISMUTH PHOSPHATE

RxCUI 2600775

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Z9P58L0522",
    "rxcui": "2600775",
    "inchikey": "SFOQXWSZZPWNCL-UHFFFAOYSA-K",
    "display_name": "BISMUTH PHOSPHATE",
    "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": "37662-0019_df26771d-0d69-dcbd-e053-2a95a90a8520",
  "productndc": "37662-0019",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BISMUTH PHOSPHATE",
  "proprietary_name": "Bismuthum Phosphoricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Bismuthum Phosphoricum",
  "start_marketing_date": "20220516",
  "active_numerator_strength": "100"
}

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