Label: MILK OF MAGNESIA LIQUID suspension
- NDC Code(s): 0904-7327-62, 0904-7327-73
- Packager: MAJOR® PHARMACEUTICALS
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 17, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each 30 mL)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
• kidney disease • a sudden change in bowel habits that lasts over 14 days
• a magnesium-restricted diet • stomach pain, nausea, or vomiting
Ask a doctor or pharmacist before use if you aretaking another medication.
This product may interact with certain medications.
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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 (8oz) of liquid with each dose
age dose Adults and children over 12 years of age 30 mL, not more than 60mL in 24 hrs Children under 6 years of age Do not use unless directed by a doctor - Other information
- Inactive ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MILK OF MAGNESIA LIQUID
milk of magnesia liquid suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-7327 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 2400 mg in 30 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0904-7327-73 10 in 1 CASE 04/17/2024 1 10 in 1 TRAY 1 NDC:0904-7327-62 30 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 04/17/2024 Labeler - MAJOR® PHARMACEUTICALS (191427277)