Label: REGULAR STRENGTH ANTACID- aluminum hydroxide, magnesium hydroxide, dimethicone liquid
- NDC Code(s): 68788-7841-3
- Packager: Preferred Pharmaceuticals Inc.
- This is a repackaged label.
- Source NDC Code(s): 46122-433
- Category: HUMAN OTC DRUG LABEL
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 July 11, 2023
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- Official Label (Printer Friendly)
- Active ingredients (in each 5 mL teaspoonful)
- Purposes
- Uses
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Warnings
Ask a doctor before use if you have
- •
- kidney disease
- •
- a magnesium-restricted diet
Ask a doctor or pharmacist before use if you are taking a prescription drug.
Antacids may interact with certain prescription drugs.
Stop use and ask a doctor if symptoms last more than 2 weeks
If pregnant or breast-feeding, ask a health professional before use. - Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
package Label
Compare to Mylanta®
Regular Strength
active ingredients*
NDC 68788-7841-3GOOD NEIGHBOR PHARMACY
Relabeled By: Preferred Pharmaceuticals Inc.
regular strengthAntacid Liquid
Alumina, Magnesia and Simethicone Oral Suspension
fast relief of
HEARTBURN
SOUR STOMACH
ACID INDIGESTION
PRESSURE AND BLOATING
ORIGINAL FLAVORAlcohol:0.15%
12 FL OZ (355 mL)
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INGREDIENTS AND APPEARANCE
REGULAR STRENGTH ANTACID
aluminum hydroxide, magnesium hydroxide, dimethicone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68788-7841(NDC:46122-433) 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, HYDROXIDE ION - UNII:9159UV381P) 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) BUTYLPARABEN (UNII: 3QPI1U3FV8) HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) Product Characteristics Color Score Shape Size Flavor LEMON (lemon) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68788-7841-3 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 01/19/2021 Labeler - Preferred Pharmaceuticals Inc. (791119022) Registrant - Preferred Pharmaceuticals Inc. (791119022) Establishment Name Address ID/FEI Business Operations Preferred Pharmaceuticals Inc. 791119022 RELABEL(68788-7841)
