Cuprum metallicum

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220161341
80 PELLET in 1 TUBE (0220-1613-41)

Annotations

UNII (FDA Substance ID)

789U1901C5

COPPER

RxCUI 2837

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "789U1901C5",
    "rxcui": "2837",
    "inchikey": "RYGMFSIKBFXOCR-UHFFFAOYSA-N",
    "display_name": "COPPER",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4b348c61-01cc-641a-e063-6294a90a53e7": {
      "match": "brand_token",
      "title": "CUPRUM METALLICUM LIQUID [NEWTON LABORATORIES, INC.]",
      "spl_version": "1",
      "published_date": "2026-02-23"
    }
  },
  "productid": "0220-1613_0a0c482e-b1a0-9bf6-e063-6394a90a70cf",
  "productndc": "0220-1613",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "COPPER",
  "proprietary_name": "Cuprum metallicum",
  "active_ingred_unit": "[hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "COPPER",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "8"
}

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