Home NDC 79481-0655 ANTACID AND ANTIGAS
Product NDC 79481-0655
11-digit product format 794810655
Labeler code 79481
Product ID 79481-0655_46a3a3ab-710e-1515-e063-6294a90adb64
Type HUMAN OTC DRUG
Nonproprietary name calcium carbonate, magnesium hydroxide, simethicone
Dosage form LIQUID
Route ORAL
Labeler Meijer, Inc.
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-01
Substance CALCIUM CARBONATE; DIMETHICONE; MAGNESIUM HYDROXIDE
Active strength 800; 80; 270 mg/10mL; mg/10mL; mg/10mL
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], 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], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], 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 AND ANTIGAS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 800 mg/10mL DIMETHICONE 80 mg/10mL MAGNESIUM HYDROXIDE 270 mg/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK Internal UNII lookup 92RU3N3Y1O Internal UNII lookup NBZ3QY004S Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1788932 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 79481-0655-1 ANTACID AND ANTIGAS 355 mL in 1 BOTTLE LIQUID 355 2
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 11 of 36 · 719 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79481-0655-1 79481065501 355 mL in 1 BOTTLE (79481-0655-1) 355 ml 2025-12-01 No No Current