Home NDC 69842-508 Antacid
Product NDC 69842-508
11-digit product format 698420508
Labeler code 69842
Product ID 69842-508_3557256e-e823-4bb3-85db-ca11abbea728
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Hydroxide, Magnesium Hydroxide and Simethicone
Dosage form SUSPENSION
Route ORAL
Labeler CVS
Application part332
Marketing category OTC MONOGRAPH FINAL
Marketing start 2011-03-09
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE
Active strength 400; 400; 40 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Antacid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 400 mg/5mL MAGNESIUM HYDROXIDE 400 mg/5mL DIMETHICONE 40 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup NBZ3QY004S Internal UNII lookup 92RU3N3Y1O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 237870 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69842-508-05 Antacid 355 mL in 1 BOTTLE SUSPENSION 355 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-508 ANTACID (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE AND SIMETHICONE) SUSPENSION [CVS] 1 Current NDC, Legacy NDC, 1 package rows 20170809_d97cd600-6fc4-4d39-9e41-344e44646506.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Antacid ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE AND SIMETHICONE CVS d97cd600-6fc4-4d39-9e41-344e44646506 2017-08-09 Warnings Exact identifier ndc (product): 69842-508
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69842-508-05 69842050805 355 mL in 1 BOTTLE (69842-508-05) 355 ml 2011-03-09 0000-00-00 No No Current