MILK OF MAGNESIA- magnesium hydroxide liquid 
AMERISOURCEBERGEN DRUG CORPORATION

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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GNP milk of mag original

Active ingredient (in each 15 mL, 1 Tablespoon)

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 over 14 days

Ask a doctor or pharmacist before use if you are 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

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

Inactive ingredients

purified water, sodium hypochlorite

Questions or Comments?

1-800-540-3765

package label

1

MILK OF MAGNESIA 
magnesium hydroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-437
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-437-40355 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33409/01/2017
Labeler - AMERISOURCEBERGEN DRUG CORPORATION (007914906)
Registrant - GCP Laboratories (965480861)
Establishment
NameAddressID/FEIBusiness Operations
GCP Laboratories965480861manufacture(46122-437) , relabel(46122-437)

Revised: 12/2021
Document Id: d346bd73-748b-7c6c-e053-2a95a90aac85
Set id: 5d690d82-e4fb-57ad-e053-2a91aa0a38ea
Version: 2
Effective Time: 20211216
 
AMERISOURCEBERGEN DRUG CORPORATION