Cobaltum 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
3766211201
200 PELLET in 1 VIAL, GLASS (37662-1120-1)
ndc11
3766211202
500 PELLET in 1 VIAL, GLASS (37662-1120-2)
ndc11
3766211203
3000 PELLET in 1 BOTTLE, GLASS (37662-1120-3)
ndc11
3766211204
10000 PELLET in 1 BOTTLE, GLASS (37662-1120-4)

Annotations

UNII (FDA Substance ID)

0B5M38T47H

COBALTOUS PHOSPHATE

RxCUI 2624688

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "0B5M38T47H",
    "rxcui": "2624688",
    "inchikey": "ZBDSFTZNNQNSQM-UHFFFAOYSA-H",
    "display_name": "COBALTOUS PHOSPHATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3b3d1223-d611-4ef2-e063-6394a90a28cc": {
      "match": "brand_token",
      "title": "COBALTUM METALLICUM (COBALT) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-19"
    }
  },
  "productid": "37662-1120_e4fdabac-edc0-bb14-e053-2a95a90aab7e",
  "productndc": "37662-1120",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "COBALTOUS PHOSPHATE",
  "proprietary_name": "Cobaltum Phosphoricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cobaltum Phosphoricum",
  "start_marketing_date": "20220729",
  "active_numerator_strength": "500"
}

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