MedPath

Aluminium

Generic Name
Aluminium
Drug Type
Small Molecule
Chemical Formula
Al
CAS Number
7429-90-5
Unique Ingredient Identifier
CPD4NFA903

Overview

A metallic element that has the atomic number 13, atomic symbol Al, and atomic weight 26.98.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Research Report

Published: Sep 26, 2025

An Analysis of Aluminum and its Compounds in Pharmaceutical Applications

Introduction: Defining Aluminum in a Medicinal Context

Clarification of Identity: Addressing the Revoked DrugBank ID and Establishing Focus on Aluminum (CAS 7429-90-5) and its Compounds

The initial query identifies the substance of interest by the DrugBank accession number DB01370. A critical preliminary finding is that this specific record has been revoked by the database curators.[1] This revocation indicates that classifying elemental aluminum as a single, discrete "small molecule" drug is pharmacologically imprecise from the perspective of modern drug information systems. The therapeutic and toxicological properties attributed to "aluminum" are not derived from the metallic element itself but from a diverse family of its inorganic compounds.

Therefore, this report will focus on elemental aluminum, identified by its Chemical Abstracts Service (CAS) number 7429-90-5, as the parent entity from which various pharmaceutically active compounds are derived.[2] The primary objective is to provide a comprehensive analysis of this family of aluminum-containing pharmaceuticals, clarifying their distinct chemical identities, therapeutic applications, mechanisms of action, and associated risks. This approach corrects the initial premise of a single drug entity and frames the subject in a scientifically accurate context.

The Dual Nature of Aluminum: A Ubiquitous Element, Versatile Pharmaceutical Ingredient, and Recognized Toxicant

Aluminum is the third most abundant element in the Earth's crust, constituting over 8% of its mass.[5] Its ubiquity ensures that human exposure through food, drinking water, and the environment is constant and unavoidable.[7] Despite this widespread presence, aluminum has no established essential biological function in humans.[5]

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/11/08
Phase 1
Recruiting
2024/09/26
Phase 1
Not yet recruiting
2024/02/20
Phase 1
Withdrawn
2023/03/23
Phase 1
Completed
2022/04/25
Phase 4
Completed
Centro de Investigacao em Saude de Manhica
2021/11/23
Phase 3
Completed
El Instituto Nacional de Neurologia y Neurocirugia Manuel Velasco Suarez
2021/06/07
Phase 1
Completed
2020/02/10
Phase 2
Completed
2018/11/28
Phase 2
Completed
Shanghai Institute Of Biological Products
2018/01/31
Phase 1
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Deseret Biologicals, Inc.
43742-1312
ORAL
12 [hp_X] in 1 mL
5/27/2025
Dr. Donna Restivo DC
62185-0062
ORAL
12 [hp_X] in 1 mL
5/23/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
MECLOSIL TABLET
SIN10845P
TABLET
325 mg
3/25/1999
MAGNESIUM TRISILICATE COMPOUND TABLET BP
SIN06599P
TABLET
120 mg
10/1/1991
GERSKIN TABLET
SIN07893P
TABLET
200 mg
10/31/1994

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
TRI-MAG-GEL B TAB
N/A
N/A
N/A
7/23/1981
XYLMOL SUPPOSITORY
N/A
N/A
N/A
6/29/2000

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
ALUMINIUM METALLICUM
dolisos canada inc.
02234297
Liquid ,  Globules ,  Granules - Oral
6 X
1/5/1998
ECZ HP
bio active canada ltd.
02233603
Liquid - Oral
30 X
5/26/1998
ALUMINIUM-INJEEL LIQ (D10-D200)
02037017
Liquid - Oral
10 D / ML
12/31/1993
UNDA 33
seroyal international inc.
02233255
Granules ,  Pellet ,  Tablet ,  Drops ,  Liquid - Oral
12 X
4/6/1998
UNDA 18
seroyal international inc.
02233233
Liquid ,  Pellet ,  Granules ,  Drops ,  Tablet - Oral
12 X
4/6/1998
UNDA 19
seroyal international inc.
02233234
Liquid ,  Tablet ,  Granules ,  Drops ,  Pellet - Oral
12 X
4/6/1998
ALUMINIUM METALLICUM GRANULE 6DH-30DH
homeocan inc.
01932861
Tablet - Oral
6 DH
12/31/1991
UNDA 43
seroyal international inc.
02233260
Liquid ,  Drops ,  Tablet ,  Pellet ,  Granules - Oral
12 X
4/6/1998
UNDA 28
seroyal international inc.
02233249
Pellet ,  Drops ,  Liquid ,  Granules ,  Tablet - Oral
12 X
4/6/1998
ALUMINIUM METALLICUM
homeocan inc.
02233882
Globules ,  Drops ,  Granules - Oral
6 X
1/24/1998

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
AVAXIM JUNIOR SUSPENSION INYECTABLE EN JERINGA PRECARGADA
85769
SUSPENSIÓN INYECTABLE EN JERINGA PRECARGADA
Medicamento Sujeto A Prescripción Médica
Not Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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