Home NDC 51316-515 Supreme Antacid Cherry
Product NDC 51316-515
11-digit product format 513160515
Labeler code 51316
Product ID 51316-515_2107f543-71e7-4c2a-9e02-1632109e1013
Type HUMAN OTC DRUG
Nonproprietary name calcium carbonate, magnesium hydroxide
Dosage form LIQUID
Route ORAL
Labeler CVS
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-28
Substance MAGNESIUM HYDROXIDE; CALCIUM CARBONATE
Active strength 135; 400 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 2027-12-31
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 Cherry
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM HYDROXIDE 135 mg/5mL CALCIUM CARBONATE 400 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination NBZ3QY004S Internal UNII lookup H0G9379FGK 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 51316-515-05 Supreme Antacid Cherry 355 mL in 1 BOTTLE LIQUID 355 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51316-515 SUPREME ANTACID CHERRY (CALCIUM CARBONATE, MAGNESIUM HYDROXIDE) LIQUID [CVS] 2 Current NDC, 1 package rows 20250130_2bc4ad16-57a1-b585-e063-6394a90a5726.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 10 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 Sample Exclude flag Status 51316-515-05 51316051505 355 mL in 1 BOTTLE (51316-515-05) 355 ml 2025-01-28 No No Current