Cuprum Iodatum

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 · 3

ndc11
3766210841
200 PELLET in 1 VIAL, GLASS (37662-1084-1)
ndc11
3766210842
1200 PELLET in 1 BOTTLE, GLASS (37662-1084-2)
ndc11
3766210843
4000 PELLET in 1 BOTTLE, GLASS (37662-1084-3)

Annotations

UNII (FDA Substance ID)

7DE9CA6IL2

CUPROUS IODIDE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7DE9CA6IL2",
    "rxcui": null,
    "inchikey": "LSXDOTMGLUJQCM-UHFFFAOYSA-M",
    "display_name": "CUPROUS IODIDE",
    "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": "37662-1084_e4e80242-9a46-5166-e053-2995a90a55e8",
  "productndc": "37662-1084",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CUPROUS IODIDE",
  "proprietary_name": "Cuprum Iodatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Iodatum",
  "start_marketing_date": "20220728",
  "active_numerator_strength": "6"
}

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