Label: GOOD SENSE ANTACID MAXIMUM STRENGTH- aluminum hydroxide, magnesium hydroxide, simethicone suspension
- NDC Code(s): 0113-0588-40
- Packager: L. Perrigo Company
- Category: HUMAN OTC DRUG LABEL
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Updated July 8, 2019
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- Active ingredients (in each 10 mL)
Ask a doctor or pharmacist before use if you are
presently taking a prescription drug. Antacids may interact with certain prescription drugs.
When using this product
do not take more than 40 mL in a 24-hour period, or use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician
- shake well before using
- only use the dose cup provided
- adults and children 12 years and older: take 10 mL to 20 mL two times a day or as directed by a physician
- do not take more than 40 mL in 24 hours or use the maximum dosage for more than 2 weeks
- children under 12 years: consult a physician
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
INGREDIENTS AND APPEARANCE
GOOD SENSE ANTACID MAXIMUM STRENGTH
aluminum hydroxide, magnesium hydroxide, simethicone suspension
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-0588 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 800 mg in 10 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 800 mg in 10 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg in 10 mL Inactive Ingredients Ingredient Name Strength BUTYLPARABEN (UNII: 3QPI1U3FV8) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color WHITE (opaque) Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0113-0588-40 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/13/2006 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part332 02/13/2006 Labeler - L. Perrigo Company (006013346)