Home NDC 0135-0095 GAVISCON
Product NDC 0135-0095
11-digit product format 001350095
Labeler code 0135
Product ID 0135-0095_4aba2043-4dde-0c18-e063-6294a90a5fcf
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide and magnesium carbonate
Dosage form LIQUID
Route ORAL
Labeler Haleon US Holdings LLC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-01-14
Substance ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
Active strength 254; 237.5 mg/5mL; mg/5mL
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 GAVISCON
Listing expiration 2027-12-31 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 · 4 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 245001 Internal RxNorm lookup 252203 Internal RxNorm lookup 404472 Internal RxNorm lookup 1251365 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 0135-0095-41 GAVISCON 355 mL in 1 BOTTLE LIQUID 355 23
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-0095 GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) LIQUID [HALEON US HOLDINGS LLC] 16 Current NDC, Legacy NDC, 1 package rows 20250529_2d74e5bc-1f10-4fb6-9258-cd906e360013.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 0135-0095-41 00135009541 355 mL in 1 BOTTLE (0135-0095-41) 355 ml 2011-01-14 0000-00-00 No No Current