Label: MILK OF MAGNESIA MINT- magnesium hydroxide liquid
- NDC Code(s): 68788-8638-3
- Packager: Preferred Pharmaceuticals Inc.
- This is a repackaged label.
- Source NDC Code(s): 57896-647
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 18, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient (in each 15 mL tablespoonful)
- Purpose
- Uses
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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 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
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- you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.
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- you need to use a laxative for more than 1 week
If pregnant or breast-feeding, ask a health professional before use.
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Directions
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- shake well before use
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- do not exceed the maximum recommended daily dose in a 24 hour period
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- dose may be taken once a day preferably at bedtime, in divided doses, or as directed by a doctor
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- drink a full glass (8 oz) of liquid with each dose
adults and children 12 years and older
2 to 4 tablespoonfuls
children 6 to 11 years
1 to 2 tablespoonfuls
children under 6 years
ask a doctor
- Other information
- Inactive ingredients
- package Label
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INGREDIENTS AND APPEARANCE
MILK OF MAGNESIA MINT
magnesium hydroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68788-8638(NDC:57896-647) 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 WATER (UNII: 059QF0KO0R) SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Product Characteristics Color Score Shape Size Flavor MINT (mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68788-8638-3 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 04/18/2024 Labeler - Preferred Pharmaceuticals Inc. (791119022) Registrant - Preferred Pharmaceuticals Inc. (791119022) Establishment Name Address ID/FEI Business Operations Preferred Pharmaceuticals Inc. 791119022 RELABEL(68788-8638)
