Label: ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND DIMETHICONE suspension
- NDC Code(s): 60687-888-45, 60687-888-51, 60687-888-76
- Packager: American Health Packaging
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 15, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients (in each 30 mL cup)
- Purpose
- Uses
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Warnings
Do not take more than 2 unit dose cups (60 mL) in a 24-hour period or use the maximum dosage for more than 2 weeks except under the advice and supervision of a physician.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Distributed by:
-
Principal Display Panel – Tray Label

Case NDC 60687-888-76/Cup NDC 60687-888-45
Magnesium Hydroxide,
Aluminum Hydroxide, and
Simethicone Suspension
Antacid/Antigas2400 mg/2400 mg/240 mg per 30 mL
Sugar Free
SHAKE WELL
USUAL DOSAGE: See attached Drug Facts
Store at 20° to 25°C (68° to 77°F)
[See USP Controlled Room Temperature].
Protect from freezing.For Institutional Use Only
T1762C300125 R01/25
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Principal Display Panel – Cup – 2400 mg/2400 mg/240 mg 30 mL

NDC 60687- 888-45
Magnesium Hydroxide,
Aluminum Hydroxide, and
Simethicone SuspensionAntacid/Anti-Gas
2400 mg/2400 mg/240 mg per 30 mL
Sugar Free
Delivers 30 mL
SHAKE WELL/Protect from freezing
See package Drug Facts insert for full
prescribing information and storage.For Institutional Use Only.
American Health Packaging
Columbus, OH 43217F1762C300125
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INGREDIENTS AND APPEARANCE
ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND DIMETHICONE
aluminum hydroxide, magnesium hydroxide, and dimethicone suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60687-888 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 5 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 400 mg in 5 mL DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O) (DIMETHICONE, UNSPECIFIED - UNII:92RU3N3Y1O) DIMETHICONE, UNSPECIFIED 40 mg in 5 mL Inactive Ingredients Ingredient Name Strength BUTYLPARABEN (UNII: 3QPI1U3FV8) PROPYLPARABEN (UNII: Z8IX2SC1OH) HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) PEPPERMINT OIL (UNII: AV092KU4JH) CYCLOMETHICONE 4 (UNII: CZ227117JE) WATER (UNII: 059QF0KO0R) 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:60687-888-76 10 in 1 CASE 07/15/2025 1 NDC:60687-888-51 10 in 1 TRAY 1 NDC:60687-888-45 30 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M002 07/15/2025 Labeler - American Health Packaging (929561009)
