INON- aluminum hydroxide, magnesium carbonate, sodium bicarbonate granule 
Sato Pharmaceutical Co., Ltd.

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Inon Granules

Active ingredients [in each packet (1.92g)]
Aluminum hydroxide 400 mg
Magnesium carbonate 400 mg
Sodium bicarbonate 700 mg

Purpose
Aluminum hydroxide     Antacid
Magnesium carbonate     Antacid
Sodium bicarbonate     Antacid

Uses relieves these symptoms
■ heartburn    ■ sour stomach    ■ acid indigestion

Warnings

If pregnant or breast-feeding, ask a health professional before use.

When using this product

■ Do not take more than 3 packets in 24-hours period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor

■ May have laxative effect


Ask a doctor before use if you have

■ a sodium-restricted diet

Ask a doctor or pharmacist before use if you are

■ taking a prescription drug Antacids may interact with certain prescription drugs.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions
■ Adults and children 12 years of age and over: Take 1 packet at a time 3 times daily between meals or after meals, or as directed by a doctor
■ Children under 12 years: Ask a doctor

Other information ■ Each packet contains: sodium 175 mg, magnesium 95 mg

Inactive ingredients  colloidal silicon dioxide, flavor, partially hydrolyzed polyvinyl alcohol, sugar, starch

inongrancart.jpg carton


INON 
aluminum hydroxide, magnesium carbonate, sodium bicarbonate granule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-045
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE400 mg  in 1.92 g
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE400 mg  in 1.92 g
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE700 mg  in 1.92 g
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
POLYVINYL ALCOHOL (UNII: 532B59J990)  
SUCROSE (UNII: C151H8M554)  
STARCH, POTATO (UNII: 8I089SAH3T)  
Product Characteristics
Color    Score    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49873-045-0112 in 1 CARTON05/31/1989
11.92 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00105/31/1989
Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
Establishment
NameAddressID/FEIBusiness Operations
Sato Pharmaceutical Co., Ltd.715699133manufacture(49873-045) , label(49873-045) , pack(49873-045)

Revised: 12/2023
Document Id: 0bb8901e-89d2-b026-e063-6294a90ae77a
Set id: e86d9c57-c877-49f1-a405-95a9a226ccf3
Version: 4
Effective Time: 20231204
 
Sato Pharmaceutical Co., Ltd.