Home NDC 0363-7630 Walgreens Fast Acting Heartburn Relief Extra Strength
Product NDC 0363-7630
11-digit product format 003637630
Labeler code 0363
Product ID 0363-7630_447ce367-bceb-756d-e063-6294a90a4bb7
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide and magnesium carbonate
Dosage form LIQUID
Route ORAL
Labeler WALGREEN CO.
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-01-15
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 Walgreens Fast Acting Heartburn Relief Extra Strength
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 0363-7630-12 Walgreens Fast Acting Heartburn Relief Extra Strength 355 mL in 1 BOTTLE LIQUID 355 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-7630 WALGREENS FAST ACTING HEARTBURN RELIEF EXTRA STRENGTH (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) LIQUID [WALGREEN CO.] 7 Current NDC, Legacy NDC, 1 package rows 20241114_6eae97f3-a174-4cbc-badc-777475d2f7af.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 Marketing end Sample Exclude flag Status 0363-7630-12 00363763012 355 mL in 1 BOTTLE (0363-7630-12) 355 ml 2018-01-15 0000-00-00 No No Current