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 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 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