Label: MAGNESIUM OXIDE 400MG tablet
- NDC Code(s): 68210-4105-1
- Packager: Spirit Pharmaceuticals LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- ACTIVE INGREDIENT (In each tablet)
- USES
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WARNINGS
Ask a doctor or pharmacist before use if you are
taking a prescription drug. Antacids may interact with certain prescription drugs.
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
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- PDP
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INGREDIENTS AND APPEARANCE
MAGNESIUM OXIDE 400MG
magnesium oxide 400mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68210-4105 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM OXIDE (UNII: 3A3U0GI71G) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM OXIDE 400 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape ROUND Size 11mm Flavor Imprint Code 174 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68210-4105-1 75 in 1 BOTTLE; Type 0: Not a Combination Product 07/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 07/02/2020 Labeler - Spirit Pharmaceuticals LLC (179621011)