Cuprum Fluoratum

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
3766209521
200 PELLET in 1 VIAL, GLASS (37662-0952-1)
ndc11
3766209522
500 PELLET in 1 VIAL, GLASS (37662-0952-2)
ndc11
3766209523
3000 PELLET in 1 BOTTLE, GLASS (37662-0952-3)
ndc11
3766209524
10000 PELLET in 1 BOTTLE, GLASS (37662-0952-4)

Annotations

UNII (FDA Substance ID)

3A38PC42E9

CUPRIC FLUORIDE DIHYDRATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "3A38PC42E9",
    "rxcui": null,
    "inchikey": "CTRICEWDSISGPV-UHFFFAOYSA-L",
    "display_name": "CUPRIC FLUORIDE DIHYDRATE",
    "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": "37662-0952_e41df23b-1102-68fa-e053-2995a90a667b",
  "productndc": "37662-0952",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CUPRIC FLUORIDE DIHYDRATE",
  "proprietary_name": "Cuprum Fluoratum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Fluoratum",
  "start_marketing_date": "20220718",
  "active_numerator_strength": "100"
}

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