Home NDC 60687-888 Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone
Product NDC 60687-888
11-digit product format 606870888
Labeler code 60687
Product ID 60687-888_39fbaa0c-00d4-898a-e063-6394a90a5a7e
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone
Dosage form SUSPENSION
Route ORAL
Labeler American Health Packaging
Application M002
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-15
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE, UNSPECIFIED
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 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 Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 400 mg/5mL MAGNESIUM HYDROXIDE 400 mg/5mL DIMETHICONE, UNSPECIFIED 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 60687-888-45 Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone 30 mL in 1 CUP, UNIT-DOSE SUSPENSION 30 2 60687-888-51 Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone 10 in 1 TRAY SUSPENSION 10 2 60687-888-76 Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone 10 in 1 CASE SUSPENSION 10 2
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 13 · 255 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 60687-888-45 60687088845 30 mL in 1 CUP, UNIT-DOSE 30 ml Historical 60687-888-51 60687088851 10 in 1 TRAY Historical 60687-888-76 60687088876 10 TRAY in 1 CASE (60687-888-76) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-888-51) / 30 mL in 1 CUP, UNIT-DOSE (60687-888-45) 10 tray 2025-07-15 No No Current