Description

Almagel-Neo is a well-established pharmaceutical-grade antacid and adsorbent formulation, widely recognized for its efficacy in gastrointestinal applications. Its primary value lies in providing rapid and reliable relief from hyperacidity and related digestive discomfort by neutralizing gastric acid and protecting the mucosal lining. This product is essential for manufacturers in the pharmaceutical industry, particularly those producing over-the-counter (OTC) medicines, veterinary pharmaceuticals, and specialized gastrointestinal treatments. Its consistent quality and proven performance make it a trusted excipient and active ingredient for formulators worldwide.

Application

• Pharmaceutical Antacid Formulations: Core ingredient in suspensions, tablets, and chewables for the treatment of heartburn, acid indigestion, and gastroesophageal reflux disease (GERD).
• Veterinary Medicinal Products: Used in remedies for digestive upset, acidosis, and ulcer management in livestock and companion animals.
• GI Protectant and Adsorbent: Employed in formulations designed to coat the stomach lining and adsorb toxins or irritants.
• Over-the-Counter (OTC) Drug Manufacturing: A key component in mass-market digestive health products due to its safety profile and effectiveness.
• Compound Pharmacy Preparations: Serves as a base material for customized medication compounding where specific antacid properties are required.
• Dietary Supplement Excipient: Can be used as an inert carrier or stabilizing agent in certain supplement formats.

Basic Information

Product Name	Almagel-Neo
CAS No.	8065-58-5
Molecular Formula	Complex Mixture
Molecular Weight	N/A (Mixture)
Synonyms	Almagel
Almagelum
Aluminum Hydroxide and Magnesium Hydroxide Mixture
Aluminum Magnesium Hydroxide
Antacid Gel (Aluminum-Magnesium)
Magaldrate (related antacid)
Aluminum Hydroxide-Magnesium Hydroxide Co-dried Gel
EINECS	Contact for details

Quality Control

Our Almagel-Neo is manufactured under strict quality management systems to ensure it meets the high standards required for pharmaceutical use. Production adheres to current Good Manufacturing Practices (cGMP) and is subject to rigorous in-process and final product testing. Key parameters such as acid-neutralizing capacity, viscosity, and microbial limits are strictly controlled. A comprehensive Certificate of Analysis (COA), detailing all test results against relevant pharmacopoeial standards (such as USP/NF or Ph. Eur.), is provided with each batch to guarantee traceability, purity, and consistent performance.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature, ideally between 15°C and 25°C (59°F and 77°F). The product should be kept in a dry, well-ventilated area away from strong odors and incompatible materials. Keep the container securely sealed when not in use to prevent contamination or moisture absorption.

Specification

Item	Specification
Description	White or almost white, viscous suspension
Identification (IR)	Conforms to standard
Assay (Al2O3)	3.50 - 4.50 % w/w
Assay (MgO)	1.20 - 2.20 % w/w
Acid Neutralizing Capacity	NLT 25.0 mEq per 5 mL
pH (5% aqueous dispersion)	7.0 - 8.5
Microbial Limits	Meets Ph. Eur./USP requirements
Heavy Metals	< 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.