Label: MAG-AL LIQUID- aluminum hydroxide and magnesium hydroxide suspension
- NDC Code(s): 0121-1760-30
- Packager: PAI Holdings, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 8, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
Do not takemore than 16 teaspoonfuls in a 24-hour period or use the maximum dosage for more than 2 weeks except under the advice and supervision of a physician.
- Directions
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Other information
- each 5 mL contains:magnesium 83 mg, sodium 1.34 mg
- does not meet USP requirements for preservative effectiveness
- store at controlled room temperature 20° - 25°C (68° - 77°F)
- protect from freezing
- White colored, peppermint flavored liquid supplied in the following oral dosage form:
NDC 0121-1760-30: 30 mL unit dose cup, in a tray of ten cups. - Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 mL Dose Cup Tray Label
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INGREDIENTS AND APPEARANCE
MAG-AL LIQUID
aluminum hydroxide and magnesium hydroxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0121-1760 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 200 mg in 5 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 200 mg in 5 mL Inactive Ingredients Ingredient Name Strength BUTYLPARABEN (UNII: 3QPI1U3FV8) PROPYLPARABEN (UNII: Z8IX2SC1OH) HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) PEPPERMINT OIL (UNII: AV092KU4JH) CYCLOMETHICONE 4 (UNII: CZ227117JE) WATER (UNII: 059QF0KO0R) Product Characteristics Color white Score Shape Size Flavor PEPPERMINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0121-1760-30 10 in 1 CASE 01/14/2004 1 10 in 1 TRAY 1 30 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 01/14/2004 Labeler - PAI Holdings, LLC (044940096) Establishment Name Address ID/FEI Business Operations PAI Holdings, LLC dba Pharmaceutical Associates, Inc. 097630693 manufacture(0121-1760)