Label: MILK OF MAGNESIA ORIGINAL- magnesium hydroxide liquid
- NDC Code(s): 62011-0124-1
- Packager: STRATEGIC SOURCING SERVICES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Updated November 7, 2023
If you are a consumer or patient please visit this version.
- Active ingredient (in each 15 mL tablespoonful)
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 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.
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.
- 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
- follow each dosage with a full glass (8 oz) of fluid
- use dosage cup provided
- tbsp = tablespoon
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
- Inactive ingredients
- package Label
INGREDIENTS AND APPEARANCE
MILK OF MAGNESIA ORIGINAL
magnesium hydroxide liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62011-0124 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62011-0124-1 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 04/01/2012 03/01/2025 Labeler - STRATEGIC SOURCING SERVICES LLC (116956644) Registrant - GCP Laboratories (965480861) Establishment Name Address ID/FEI Business Operations GCP Laboratories 965480861 manufacture(62011-0124)