Label: ANTACID AND GASRELIEF- aluminum hydroxide, magnesium hydroxide, dimethicone suspension
- NDC Code(s): 50804-629-12
- Packager: GOODSENSE
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 10, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each 10 mL dose)
- Purposes
- Uses
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Warnings
Ask a doctor before use if you have
• kidney disease
• a magnesium-restricted dietAsk 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.
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Directions
- shake well before use
- adults and children 12 years of age and older: take 10 mL to 20 mL (1 to 2 doses) between meals as needed, at bedtime, or as directed by a doctor
- do not exceed 120 mL (12 doses) in a 24 hour period or use the maximum dosage for more than 2 weeks
- children under 12 years of age: ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
- package label
-
INGREDIENTS AND APPEARANCE
ANTACID AND GASRELIEF
aluminum hydroxide, magnesium hydroxide, dimethicone suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-629 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 400 mg in 10 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 400 mg in 10 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 40 mg in 10 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) BUTYLPARABEN (UNII: 3QPI1U3FV8) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL SOLUTION (UNII: 8KW3E207O2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50804-629-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 07/01/2020 Labeler - GOODSENSE (076059836) Registrant - GCP Laboratories (965480861) Establishment Name Address ID/FEI Business Operations GCP Laboratories 965480861 manufacture(50804-629)