Label: ANTACID MINT- aluminum hydroxide, magnesium hydroxide, demithicone suspension
- NDC Code(s): 0363-0432-12, 0363-0432-26
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 January 18, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if you are
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Keep out of the reach of children.
- Directions
- Other Information
- Inactive Ingredients
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Principal Display Panel
Compare to Maalox® Advanced Regular Strength Active ingredient††
Antacid +
Anti-Gas Liquid
ALUMINUM HYDROXIDE 200 mg / ANTACID
MAGNESIUM HYDROXIDE 200 mg / ANTACID
SIMETHICONE 20 mg /ANTI-GAS
REGULAR STRENGTH
- Fast relief of heartburn, pressure, bloating & acid indigestion
FL OZ (mL)
MINT FLAVOR
††This product is not manufactured or distributed by Novartis Consumer Health, Inc., distributor of Maalox® Advanced Regular Strength.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY: WALGREENS CO.,
200 WILMOT RD., DEERFIELD, IL 60015
walgreens.com
- Package Label
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INGREDIENTS AND APPEARANCE
ANTACID MINT
aluminum hydroxide, magnesium hydroxide, demithicone suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0432 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) MAGNESIUM HYDROXIDE 200 mg in 5 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 20 mg in 5 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM CITRATE (UNII: EE90ONI6FF) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0432-26 769 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/31/2018 12/29/2023 2 NDC:0363-0432-12 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/31/2018 12/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part332 03/31/2018 12/29/2024 Labeler - Walgreens (008965063)