MILK OF MAGNESIA ORIGINAL - magnesium hydroxide liquid 
ATLANTIC BIOLOGICALS CORP.

----------

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.

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

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 adults and children 12 years and older: 2 to 4 tablespoonfuls (TBSP) children 6 to 11 years: 1 to 2 tablespoonfuls (TBSP) children under 6 years: ask a doctor


Other information

• magnesium 500 mg • store at room temperature and avoid freezing • close cap tightly after use • each 15 mL tablespoonful contains:


TAMPER-EVIDENT: Do not use if imprinted neckband is missing or broken.

Inactive ingredients

purified water, sodium hypochlorite

MILK OF MAGNESIA ORIGINAL (MAGNESIUM HYDROXIDE) LIQUID

image 1
MILK OF MAGNESIA ORIGINAL  
magnesium hydroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17856-0788(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:17856-0788-110 mL in 1 CUP; Type 0: Not a Combination Product05/08/2024
2NDC:17856-0788-330 mL in 1 CUP; Type 0: Not a Combination Product05/08/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00712/08/2010
Labeler - ATLANTIC BIOLOGICALS CORP. (047437707)
Registrant - ATLANTIC BIOLOGICALS CORP. (047437707)
Establishment
NameAddressID/FEIBusiness Operations
UNIT DOSE SOLUTIONS.360804194REPACK(17856-0788)

Revised: 5/2024
Document Id: f9143617-5978-4d7d-bfad-d43d245db41b
Set id: 30fb7b5e-56a3-423e-ae57-432006b54fff
Version: 10
Effective Time: 20240508
 
ATLANTIC BIOLOGICALS CORP.