Label: MEDIBEST MILK OF MAGNESIA- magnesium hydroxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 58599-058-12 - Packager: Purine Pharma LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated September 12, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Use
- WARNINGS
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if you are
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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Directions
● 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 (8 oz) of liquid with each dose.
● mL = milliliter; TBSP = Tablespoon
adults and children 12 years and older 30 mL (2 TBSP) to 60 mL (4 TBSP) children 6 to 11 years 15 mL (1 TBSP) to 30 mL (2 TBSP) children under 6 years ask a doctor - OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEDIBEST MILK OF MAGNESIA
magnesium hydroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58599-058 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE 1200 mg in 15 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:58599-058-12 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/12/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 10/12/2016 Labeler - Purine Pharma LLC (019950491) Registrant - Purine Pharma LLC (019950491) Establishment Name Address ID/FEI Business Operations Purine Pharma LLC 019950491 manufacture(58599-058)
