Aluminium 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
3766235661
200 PELLET in 1 VIAL, GLASS (37662-3566-1)
ndc11
3766235662
500 PELLET in 1 VIAL, GLASS (37662-3566-2)
ndc11
3766235663
3000 PELLET in 1 BOTTLE, GLASS (37662-3566-3)
ndc11
3766235664
10000 PELLET in 1 BOTTLE, GLASS (37662-3566-4)

Annotations

UNII (FDA Substance ID)

Z77H3IKW94

ALUMINUM FLUORIDE

RxCUI 2273602

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Z77H3IKW94",
    "rxcui": "2273602",
    "inchikey": "KLZUFWVZNOTSEM-UHFFFAOYSA-K",
    "display_name": "ALUMINUM FLUORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a474ba15-34a5-f07e-e053-2995a90a61ca": {
      "match": "brand_token",
      "title": "ALUMINIUM SULPHURICUM PELLET [HAHNEMANN LABORATORIES, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "37662-3566_002ce4f0-e919-6409-e063-6394a90a99ed",
  "productndc": "37662-3566",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM FLUORIDE",
  "proprietary_name": "Aluminium Fluoratum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aluminium Fluoratum",
  "start_marketing_date": "20230710",
  "active_numerator_strength": "1"
}

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