Label: MAXIMUM STRENGTH ANTACID CHERRY- aluminum hydroxide, magnesium hydroxide, simethicone liquid
- NDC Code(s): 41163-065-05
- Packager: UNITED NATURAL FOODS, INC. DBA UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT (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 A DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
-
PRINCIPAL DISPLAY PANEL
compare to
MAALOX® Maximum Strength
active ingredients*
NDC 41163-065-05
EQUALINE®
maximum strength
antacid
liquid
aluminum hydroxide
800 mg/10 mL - antacid
Magnesium hydroxide
800 mg/10 mL - antacid
simethicone
80 mg/10 mL - antigas
relief of:- heartburn
- acid indigestion
- gas
Cherry Flavor
12 FL OZ (355 mL)
-
INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH ANTACID CHERRY
aluminum hydroxide, magnesium hydroxide, simethicone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-065 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 GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) 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 CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41163-065-05 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 06/10/2022 Labeler - UNITED NATURAL FOODS, INC. DBA UNFI (943556183) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 MANUFACTURE(41163-065)