Label: MILK OF MAGNESIA MINT- magnesium hydroxide liquid
- NDC Code(s): 0536-2470-83, 0536-2470-85
- Packager: Rugby Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 2, 2023
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)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- kidney disease
- a magnesium-restricted diet
- stomach pain, nausea, or vomiting
- 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
- you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.
- 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
- shake well before use
- do not exceed the maximum recommended daily dose in a 24 hour period
- dose may be taken once a day, 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 30 mL to 60 mL
children 6 to 11 years 15 mL to 30 mL children under 6 years ask a doctor - Other information
- Inactive ingredients
- package Label
-
INGREDIENTS AND APPEARANCE
MILK OF MAGNESIA MINT
magnesium hydroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0536-2470 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:0536-2470-83 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2017 05/01/2020 2 NDC:0536-2470-85 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 01/28/2011 Labeler - Rugby Laboratories (079246066) Registrant - GCP Laboratories (965480861) Establishment Name Address ID/FEI Business Operations GCP Laboratories 965480861 manufacture(0536-2470)