Label: ANTACID ANTIGAS MAXIMUM STRENGTH- aluminum hydroxide, magnesium hydroxide, simethicone liquid
- NDC Code(s): 55319-528-12
- Packager: Family Dollar (FAMILY WELLNESS)
- 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 October 31, 2022
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- Official Label (Printer Friendly)
- Active ingredient (in each 10 mL)
- Purpose
- Uses
- Warnings
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Directions
- shake well before using
- mL = milliliter
- do not take more than 60 mL in 24 hours or use the maximum dosage for more than 2 weeks
- measure only with dosing cup provided. Do not use any other dosing device
- keep dosing cup with product
- adults and children12 years and older: take 10-20 mL as needed, between or after meals, at bedtime, or as directed by a doctor
- children under 12 years of age: do not use
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
COMPARE TO THE ACTIVE INGREDIENTS IN MYLANTA® MAXIMUM STRENGTH*
MAXIMUM STRENGTH
Antacid & Anti-gas Relief
Multi-Symptom Relief
Aluminum Hydroxide - Antacid
Magnesium Hydroxide - Antacid
Simethicone - Antigas
For Fast Relief of:
- Heartburn
- Acid Indigestion
- Pressure
- Bloating
Alcohol-Free
Sugar-Free
Paraben-Free
ORIGINAL FLAVOR
*This product is not manufactured or distributed by McNeil Consumer Pharmaceuticals Co., distributor of Mylanta® Maximum Strength.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY: MIDWOOD BRANDS, LLC
10611 MONROE RD.MATTHEWS, NC 28105
- Product Label
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INGREDIENTS AND APPEARANCE
ANTACID ANTIGAS MAXIMUM STRENGTH
aluminum hydroxide, magnesium hydroxide, simethicone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55319-528 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) MAGNESIUM HYDROXIDE 800 mg in 10 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg in 10 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) GLYCERIN (UNII: PDC6A3C0OX) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) WATER (UNII: 059QF0KO0R) SODIUM CARBONATE (UNII: 45P3261C7T) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55319-528-12 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2018 06/30/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 06/30/2018 06/30/2025 Labeler - Family Dollar (FAMILY WELLNESS) (024472631)