Label: QCH MAXIMUM STRENGTH ANTACID 516- aluminum hydroxide, magnesium hydroxide, simethicone liquid
- NDC Code(s): 83324-122-12
- Packager: Chain Drug Marketing Association Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 28, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS (in each 10 mL )
- PURPOSE
- USE(S)
- WARNINGS
- ASK A DOCTOR BEFORE USE IF YOU HAVE
- ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE
- STOP USE AND ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
-
PRINCIPAL DISPLAY PANEL
NDC 83324-122-12
QCQUALITY CHOICE
*Compare to the Active Ingredients in Mylanta®Maximum Strength
Maximum StrengthAntacid Liquid
Antacid & Antigas
Aluminum Hydroxide 800 mg
Magnesium Hydroxide 800 mg
Simethicone 80 mg
Relieves:Acid Indigestion
Heartburn
Sour Stomach
Pressure & Bloating
Original Flavor
Alcohol content 0.2% v/v12 FL OZ (355 mL)
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INGREDIENTS AND APPEARANCE
QCH MAXIMUM STRENGTH ANTACID 516
aluminum hydroxide, magnesium hydroxide, simethicone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-122 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 ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) Product Characteristics Color WHITE Score Shape Size Flavor MINT (Lemon mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-122-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/28/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 08/28/2024 Labeler - Chain Drug Marketing Association Inc. (011920774) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 MANUFACTURE(83324-122)