Home NDC 57896-638 GERI-MOX MAX CHERRY
Product NDC 57896-638
11-digit product format 578960638
Labeler code 57896
Product ID 57896-638_43f770ab-1ea6-c06a-e063-6294a90aebd2
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide, magnesium hydroxide, dimethicone
Dosage form SUSPENSION
Route ORAL
Labeler Geri-Care Pharmaceuticals, Corp
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2000-01-01
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE
Active strength 400; 400; 40 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classes Calculi Dissolution Agent [EPC], 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], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 57896-638 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 57896-638 57896-638-12 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…
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 GERI-MOX MAX CHERRY
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 400 mg/5mL MAGNESIUM HYDROXIDE 400 mg/5mL DIMETHICONE 40 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup NBZ3QY004S Internal UNII lookup 92RU3N3Y1O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 237870 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 57896-638-10 GERI-MOX MAX CHERRY 30 mL in 1 CUP, UNIT-DOSE SUSPENSION 30 5 57896-638-10 GERI-MOX MAX CHERRY 100 in 1 CASE SUSPENSION 100 5 57896-638-12 GERI-MOX MAX CHERRY 355 mL in 1 BOTTLE SUSPENSION 355 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALUMINUM HYDROXIDE ACTIVE INGREDIENT 5QB0T2IUN0 GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 DIMETHICONE ACTIVE INGREDIENT 92RU3N3Y1O GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 MAGNESIUM HYDROXIDE ACTIVE INGREDIENT NBZ3QY004S GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 ALUMINUM HYDROXIDE ACTIVE MOIETY 5QB0T2IUN0 GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 DIMETHICONE ACTIVE MOIETY 92RU3N3Y1O GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 MAGNESIUM HYDROXIDE ACTIVE MOIETY NBZ3QY004S GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 BUTYLPARABEN INACTIVE INGREDIENT 3QPI1U3FV8 GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 SACCHARIN SODIUM DIHYDRATE INACTIVE INGREDIENT SB8ZUX40TY GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1 WATER INACTIVE INGREDIENT 059QF0KO0R GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57896-638 GERI-MOX MAX CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] 4 Current NDC, Legacy NDC, 3 package rows 20240823_8e57bcf5-2960-4c41-8bf2-83cb1ee50168.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 1 of 36 · 719 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Childrens Stomach Relief CALCIUM CARBONATE Wal-Mart Stores Inc 7471ec99-6c0b-40d8-a9cf-85240a0d471a 2026-09-09 Warnings Exact identifier application number: M001 Walgreens Orange Antacid Soft Chew CALCIUM CARBONATE Walgreens 5b01be31-5871-d4f5-e063-6294a90a671a 2026-09-08 Warnings Exact identifier application number: M001 Regular Strength Tropical Fruit CALCIUM CARBONATE RARITAN PHARMACEUTICALS INC 38c6cece-71a0-40d8-bfc8-2f6467f9239b 2026-09-05 Warnings Exact identifier application number: M001 Extra Strength Antacid Assorted Berries CALCIUM CARBONATE RARITAN PHARMACEUTICALS INC 07a50168-6b05-4c99-9969-7d7f0aa54f30 2026-09-05 Warnings Exact identifier application number: M001 DRx CHOICE Antacid Calcium Regular Strength CALCIUM CARBONATE 500MG Raritan Pharmaceuticals Inc 0c579405-9397-4bf2-8441-e89011b19ec4 2026-09-05 Warnings Exact identifier application number: M001 Tums Chewy Bites Wintermint and Vanilla Cream CALCIUM CARBONATE Haleon US Holdings LLC 4f094feb-8de1-4ccb-e063-6294a90acec2 2026-09-04 Warnings Exact identifier application number: M001 DG health Ultra Strength Assorted Fruit Antacid CALCIUM CARBONATE DOLGENCORP, LLC 98a0503c-add5-4453-9d9d-6f813866f4b3 2026-09-03 Warnings Exact identifier application number: M001 DG health Ultra Strength Assorted Berry Antacid CALCIUM CARBONATE DOLGENCORP, LLC 99c7ab95-df12-4041-ae1a-398cc6f0085d 2026-09-03 Warnings Exact identifier application number: M001 DG HEALTH Ultra Strength ANTACID TABLETS (CALCIUM CARBONATE) DOLGENCORP, LLC e7be2ad1-c85c-4ac7-b6e7-641f979d0d6b 2026-09-03 Warnings Exact identifier application number: M001 DG HEALTH Liquid Antacid plus Anti Gas CALCIUM CARBONATE, MAGNESIUM HYDROXIDE AND SIMETHICONE DOLGENCORP, LLC 8ecb4418-e647-49b5-b418-1c63bb3e5a3c 2026-09-03 Warnings Exact identifier application number: M001 DG health Extra Strength Antacid CALCIUM CARBONATE DOLGENCORP, LLC 4942747a-8b6c-422a-8150-9bd91c0a3778 2026-09-03 Warnings Exact identifier application number: M001 DG HEALTH Regular Strength ANTACID TABLETS (CALCIUM CARBONATE) DOLGENCORP, LLC 13dd2758-a372-4b0e-bc99-56a2dacbf95f 2026-09-03 Warnings Exact identifier application number: M001 DG health Extra Strength Antacid Wintergreen flavor CALCIUM CARBONATE DOLGENCORP, LLC b84b3509-3178-4616-9bec-dad85a4f9d2a 2026-09-03 Warnings Exact identifier application number: M001 DG Health Regular Strength Antacid CALCIUM CARBONATE DOLGENCORP, LLC 59ad3cc7-4144-442f-a37d-75c5fe23e1ae 2026-09-03 Warnings Exact identifier application number: M001 DG health Extra Strength Assorted Fruits Antacid CALCIUM CARBONATE DOLGENCORP, LLC 112f1002-c007-4363-ade6-8dfbc61f4b64 2026-09-03 Warnings Exact identifier application number: M001 DG health Extra Strength Antacid SMOOTH DISSOLVE CALCIUM CARBONATE DOLGENCORP, LLC cabaa8f7-9c93-439d-905a-5ef643a08ea8 2026-09-03 Warnings Exact identifier application number: M001 Kroger Extra Strength ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE THE KROGER CO., 175d9f0f-266a-4dc2-865f-d1ebd4ddac51 2026-09-01 Warnings Exact identifier application number: M001 Kids Antacid CALCIUM CARBONATE THE KROGER CO. d77c629b-5308-4b71-9024-9899cf88dbae 2026-09-01 Warnings Exact identifier application number: M001 Kroger Extra Strength Smooth Antacid Assorted Berry CALCIUM CARBONATE KROGER COMPANY 4c8d39d9-9d58-45df-9ffd-2cdc41539c03 2026-09-01 Warnings Exact identifier application number: M001 Kroger Ultra Strength Assorted Fruit CALCIUM CARBONATE KROGER COMPANY b60ced06-725c-4dae-abbf-21cab9e431f9 2026-08-31 Warnings Exact identifier application number: M001
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 57896-638-10 57896063810 100 CUP, UNIT-DOSE in 1 CASE (57896-638-10) / 30 mL in 1 CUP, UNIT-DOSE 2025-11-01 No No Current 57896-638-12 57896063812 355 mL in 1 BOTTLE (57896-638-12) 355 ml 2011-03-01 No No Current