MILK OF MAGNESIA ORIGINAL- magnesium hydroxide liquid 
REMEDYREPACK INC.

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.

----------

major mom

Active ingredient (in each 15 mL)

Magnesium hydroxide 1200 mg

Purpose

Saline laxative

Uses

Warnings

Ask a doctor before use if you have

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

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

adults and children 12 years and older30 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?

800-616-2471

DRUG: MILK OF MAGNESIA ORIGINAL

GENERIC: magnesium hydroxide

DOSAGE: LIQUID

ADMINSTRATION: ORAL

NDC: 70518-3351-0

NDC: 70518-3351-1

PACKAGING: 30 mL in 1 CUP, UNIT-DOSE

OUTER PACKAGING: 10 in 1 BOX

ACTIVE INGREDIENT(S):

INACTIVE INGREDIENT(S):

Remedy_Label

MM2

MILK OF MAGNESIA ORIGINAL 
magnesium hydroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70518-3351(NDC:0904-0788)
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:70518-3351-010 in 1 BOX01/31/2022
1NDC:70518-3351-130 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33401/31/2022
Labeler - REMEDYREPACK INC. (829572556)

Revised: 2/2022
Document Id: d7c4a53d-62bf-1d70-e053-2a95a90a7655
Set id: e10f3ee8-c526-40bc-b81f-46696ee310f1
Version: 1
Effective Time: 20220211
 
REMEDYREPACK INC.