Label: MILK OF MAGNESIA- magnesium hydroxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53807-125-12, 53807-125-16, 53807-125-28 - Packager: RIJ Pharmaceutical Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated April 30, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (in each 15 mL Tablespoon)
- Purpose
- Use
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Warnings
Ask a doctor before use if you have
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- kidney disease
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- a magnesium-restricted diet
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- stomach pain, nausea, or vomiting
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- a sudden change in bowel habits that lasts more than 14 days
Ask a doctor or pharmacist before use if you are
taking a prescription drug. This product may interact with certain prescription drugs.
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Directions
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- do not exceed the maximum recommended daily dose in a 24 hour period
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- shake well before use
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- 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
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- mL = milliliter, TBSP = Tablespoonful
adults and children 12 years and older
30 mL (2 TBSP) to 60 mL (4 TBSP)
children 6 to 11 years
15 mL (1 TBSP) to 30 mL (2 TBSP)
children under 6 years
ask a doctor
- Other information
- Inactive ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
MILK OF MAGNESIA
magnesium hydroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53807-125 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 1200 mg in 15 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) Product Characteristics Color WHITE (opaque) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53807-125-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/16/1999 2 NDC:53807-125-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/16/1999 3 NDC:53807-125-28 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/16/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 03/16/1999 Labeler - RIJ Pharmaceutical Corporation (144679156) Establishment Name Address ID/FEI Business Operations RIJ Pharmaceutical Corporation 144679156 manufacture(53807-125)