Home NDC 0904-7727 ACID GONE ANTACID
Product NDC 0904-7727
11-digit product format 009047727
Labeler code 0904
Product ID 0904-7727_5333826a-ab01-5e1b-e063-6394a90ac59e
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide and magnesium carbonate
Dosage form LIQUID
Route ORAL
Labeler Major Pharmaceuticals
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-12-30
Substance ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
Active strength 95; 358 mg/15mL; mg/15mL
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 ACID GONE ANTACID
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 95 mg/15mL MAGNESIUM CARBONATE 358 mg/15mL
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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 252203 Internal RxNorm lookup 1251355 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 0904-7727-14 ACID GONE ANTACID 355 mL in 1 BOTTLE LIQUID 355 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0904-7727 ACID GONE ANTACID (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) LIQUID [MAJOR PHARMACEUTICALS] 4 Current NDC, Legacy NDC, 1 package rows 20231103_3d353a92-92f1-4304-8895-31d39dccd88c.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0904-7727-14 00904772714 355 mL in 1 BOTTLE (0904-7727-14) 355 ml 2017-03-01 0000-00-00 No No Current