Cobaltum 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
3766210091
200 PELLET in 1 VIAL, GLASS (37662-1009-1)
ndc11
3766210092
500 PELLET in 1 VIAL, GLASS (37662-1009-2)
ndc11
3766210093
3000 PELLET in 1 BOTTLE, GLASS (37662-1009-3)
ndc11
3766210094
10000 PELLET in 1 BOTTLE, GLASS (37662-1009-4)

Annotations

UNII (FDA Substance ID)

USK772NS56

COBALT OXIDE

RxCUI 2606479

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "USK772NS56",
    "rxcui": "2606479",
    "inchikey": "UBEWDCMIDFGDOO-UHFFFAOYSA-N",
    "display_name": "COBALT OXIDE",
    "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": "37662-1009_e45833c5-ec2f-4ccf-e053-2a95a90ab36a",
  "productndc": "37662-1009",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "COBALT OXIDE",
  "proprietary_name": "Cobaltum Oxydatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cobaltum Oxydatum",
  "start_marketing_date": "20220721",
  "active_numerator_strength": "200"
}

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