Home NDC 63868-565 HEARTBURN RELIEF
Product NDC 63868-565
11-digit product format 638680565
Labeler code 63868
Product ID 63868-565_097f7264-6848-61fb-e063-6294a90a3f2f
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide and magnesium carbonate
Dosage form SUSPENSION
Route ORAL
Labeler CHAIN DRUG MARKETING ASSOCIATION
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-11-01
Substance ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
Active strength 254; 237.5 mg/5mL; mg/5mL
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 HEARTBURN RELIEF
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 254 mg/5mL MAGNESIUM CARBONATE 237.5 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup 0E53J927NA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 245001 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63868-565-12 HEARTBURN RELIEF 355 mL in 1 BOTTLE SUSPENSION 355 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63868-565 HEARTBURN RELIEF (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) SUSPENSION [CHAIN DRUG MARKETING ASSOCIATION] 2 Current NDC, Legacy NDC, 1 package rows 20231107_b4656a2f-a866-5f7a-e053-2995a90ac2c2.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 63868-565-12 63868056512 355 mL in 1 BOTTLE (63868-565-12) 355 ml 2019-11-01 0000-00-00 No No Current