Home NDC 55319-624 SUPREME ANTACID
Product NDC 55319-624
11-digit product format 553190624
Labeler code 55319
Product ID 55319-624_43f5b769-711e-58cf-e063-6394a90a5674
Type HUMAN OTC DRUG
Nonproprietary name calcium carbonate, magnesium hydroxide
Dosage form SUSPENSION
Route ORAL
Labeler FAMILY DOLLAR SERVICES INC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-06-01
Substance CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Active strength 400; 135 mg/5mL; mg/5mL
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], 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 SUPREME ANTACID
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 400 mg/5mL MAGNESIUM HYDROXIDE 135 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK 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 237865 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 55319-624-12 SUPREME ANTACID 355 mL in 1 BOTTLE SUSPENSION 355 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55319-624 SUPREME ANTACID (CALCIUM CARBONATE, MAGNESIUM HYDROXIDE) SUSPENSION [FAMILY DOLLAR SERVICES INC] 4 Current NDC, Legacy NDC, 1 package rows 20240201_5e996df3-25a4-b259-e053-2a91aa0a4311.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 8 of 34 · 678 matching rows.
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 55319-624-12 55319062412 355 mL in 1 BOTTLE (55319-624-12) 355 ml 2017-08-01 0000-00-00 No No Current