Label: MAGMEX- magnesium hydroxide liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 53145-060-04 - Packager: Menper Distributors, Inc.
- 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 March 14, 2014
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
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
•drink a full glass (8 oz) of liquid with each dose•for accurate dosing, use dose cup provided
•TBSP = tablespoonful
adults and children 12 years and older
2 to 4 TBSP.
children 6 to 11 years
1 to 2 TBSP.
children under 6 years
ask a doctor
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MAGMEX
magnesium hydroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53145-060 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 MINERAL OIL (UNII: T5L8T28FGP) PEPPERMINT OIL (UNII: AV092KU4JH) SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SPEARMINT (UNII: J7I2T6IV1N) WATER (UNII: 059QF0KO0R) Product Characteristics Color white Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53145-060-04 1 in 1 CARTON 1 133 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 02/21/2012 Labeler - Menper Distributors, Inc. (101947166)