SUNMARK MILK OF MAGNESIA MINT description, usages, side effects, indications, overdosage, supplying and lots more!

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SUNMARK MILK OF MAGNESIA MINT

McKesson


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each 15 mL, 1 Tablespoon)

Magnesium hydroxide 1200 mg

Purpose

Saline laxative

SUNMARK MILK OF MAGNESIA MINT Uses

  • relieves occasional constipation (irregularity)
  • generally produces bowel movement in 1/2 to 6 hours

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 2 weeks


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.


Keep this and all drugs out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center (1-800-222-1222) immediately.

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

• follow each dosage with a full glass (8 oz) of fluid

adults and children 12 years and over: 2 - 4 tablespoons (TBSP)

children 6 to 11 years: 1- 2 tablespoons (TBSP)

children under 6 years: ask a doctor


SUNMARK MILK OF MAGNESIA MINT Other information

each tablespoon contains: magnesium 500 mg

• do not freeze

• store at room temperature tightly closed

Inactive ingredients

flavor, purified water, saccharin sodium, sodium hypochlorite

Questions or Comments?

1-800-540-3765

package Label

SUNMARK MILK OF MAGNESIA MINT

SUNMARK MILK OF MAGNESIA MINT

magnesium hydroxide LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-305
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
magnesium hydroxide MAGNESIUM CATION 1200 mg

Inactive Ingredients

Ingredient Name Strength
water
SODIUM HYPOCHLORITE
SACCHARIN SODIUM DIHYDRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-305-39 355 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2012-04-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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