Mercurius Praecipitatus Ruber

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
3766238461
200 PELLET in 1 VIAL, GLASS (37662-3846-1)
ndc11
3766238462
500 PELLET in 1 VIAL, GLASS (37662-3846-2)
ndc11
3766238463
3000 PELLET in 1 BOTTLE, GLASS (37662-3846-3)
ndc11
3766238464
10000 PELLET in 1 BOTTLE, GLASS (37662-3846-4)

Annotations

UNII (FDA Substance ID)

IY191986AO

MERCURIC OXIDE

RxCUI 221122

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "IY191986AO",
    "rxcui": "221122",
    "inchikey": "QYZBCWXZSYTIOY-UHFFFAOYSA-N",
    "display_name": "MERCURIC OXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4613030f-72fc-493b-a3e3-7417888014b3": {
      "match": "brand_token",
      "title": "MERCURIUS SOLUBILIS 7127 (MERCURIUS SOLUBILIS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-3846_03b378d2-bbd7-7891-e063-6394a90a2722",
  "productndc": "37662-3846",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MERCURIC OXIDE",
  "proprietary_name": "Mercurius Praecipitatus Ruber",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Mercurius Praecipitatus Ruber",
  "start_marketing_date": "20230824",
  "active_numerator_strength": "1"
}

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