Aluminum Metallicum

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
3766227001
200 PELLET in 1 VIAL, GLASS (37662-2700-1)
ndc11
3766227002
500 PELLET in 1 VIAL, GLASS (37662-2700-2)
ndc11
3766227003
3000 PELLET in 1 BOTTLE, GLASS (37662-2700-3)
ndc11
3766227004
10000 PELLET in 1 BOTTLE, GLASS (37662-2700-4)

Annotations

UNII (FDA Substance ID)

CPD4NFA903

ALUMINUM

RxCUI 1311504

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "CPD4NFA903",
    "rxcui": "1311504",
    "inchikey": "XAGFODPZIPBFFR-UHFFFAOYSA-N",
    "display_name": "ALUMINUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "60a54d4e-89c2-4329-86bf-a288527f37b5": {
      "match": "brand_token",
      "title": "ALUMINUM HYDROXIDE (ALUMINUM HYDROXIDE) LIQUID [ATLANTIC BIOLOGICALS CORP.]",
      "spl_version": "7",
      "published_date": "2025-12-16"
    }
  },
  "productid": "37662-2700_f49f4a93-d9a7-0964-e053-2995a90a867e",
  "productndc": "37662-2700",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM",
  "proprietary_name": "Aluminum Metallicum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aluminum Metallicum",
  "start_marketing_date": "20230216",
  "active_numerator_strength": "1"
}

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