MILK OF MAGNESIA MINT- magnesium hydroxide liquid 
Chain Drug Marketing Association

----------

qc mom mint

Active ingredient (in each 15 mL)

Magnesium hydroxide 1200 mg

Purpose

Saline laxative

Uses

Warnings

Ask a doctor before use if you have

• kidney disease

• a magnesium-restricted diet

• stomach pain, nausea, or vomiting

• a sudden change in bowel habits that lasts more than 2 weeks

Ask a doctor or pharmacist before use if you are presently taking a prescription drug.

This product may interact with certain prescription drugs.

Stop use and ask a doctor if

• you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.

• you need to use a laxative for more than 1 week

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

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

Directions

• shake well before use

• do not exceed the maximum recommended daily dose in a 24 hour period

• dose may be taken once a day preferably at bedtime, in divided doses, or as directed by a doctor

• drink a full glass (8 oz) of liquid with each dose

agedose
adults and children 12 years and over30 mL to 60 mL
children 6 to 11 years15 mL to 30 mL
children under 6 yearsask a doctor

Other information

each 15 mL contains: magnesium 500 mg

• store at room temperature and avoid freezing

• close cap tightly after use

Inactive ingredients

flavor, purified water, saccharin sodium, sodium hypochlorite

package label

1

MILK OF MAGNESIA MINT 
magnesium hydroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-788
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE1200 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-788-57355 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00704/01/2014
Labeler - Chain Drug Marketing Association (011920774)
Registrant - GCP Laboratories (965480861)
Establishment
NameAddressID/FEIBusiness Operations
GCP Laboratories965480861manufacture(63868-788)

Revised: 11/2023
Document Id: 097f7264-6849-61fb-e063-6294a90a3f2f
Set id: 7722145c-913c-4ed5-a9b2-a6c343064066
Version: 4
Effective Time: 20231106
 
Chain Drug Marketing Association