Cobaltum Sulphuricum

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
3766222011
200 PELLET in 1 VIAL, GLASS (37662-2201-1)
ndc11
3766222012
500 PELLET in 1 VIAL, GLASS (37662-2201-2)
ndc11
3766222013
3000 PELLET in 1 BOTTLE, GLASS (37662-2201-3)
ndc11
3766222014
10000 PELLET in 1 BOTTLE, GLASS (37662-2201-4)

Annotations

UNII (FDA Substance ID)

Y8N698ZE0T

COBALTOUS SULFATE HEPTAHYDRATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Y8N698ZE0T",
    "rxcui": null,
    "inchikey": "MEYVLGVRTYSQHI-UHFFFAOYSA-L",
    "display_name": "COBALTOUS SULFATE HEPTAHYDRATE",
    "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": "37662-2201_f062baf5-af5e-8425-e053-2995a90a79cb",
  "productndc": "37662-2201",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "COBALTOUS SULFATE HEPTAHYDRATE",
  "proprietary_name": "Cobaltum Sulphuricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cobaltum Sulphuricum",
  "start_marketing_date": "20221222",
  "active_numerator_strength": "100"
}

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