Home NDC 0536-0091 Aluminum Hydroxide
Product NDC 0536-0091
11-digit product format 005360091
Labeler code 0536
Product ID 0536-0091_45aff4ec-4b96-2833-e063-6394a90a2f26
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide
Dosage form LIQUID
Route ORAL
Labeler Rugby Laboratories
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-02-01
Substance ALUMINUM HYDROXIDE
Active strength 320 mg/5mL
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
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 320 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308078 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 0536-0091-85 Aluminum Hydroxide 473 mL in 1 BOTTLE LIQUID 473 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALUMINUM HYDROXIDE ACTIVE INGREDIENT 5QB0T2IUN0 ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 ALUMINUM HYDROXIDE ACTIVE INGREDIENT 5QB0T2IUN0 ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 ALUMINUM HYDROXIDE ACTIVE MOIETY 5QB0T2IUN0 ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 ALUMINUM HYDROXIDE ACTIVE MOIETY 5QB0T2IUN0 ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 BUTYLPARABEN INACTIVE INGREDIENT 3QPI1U3FV8 ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 BUTYLPARABEN INACTIVE INGREDIENT 3QPI1U3FV8 ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 DIMETHICONE INACTIVE INGREDIENT 92RU3N3Y1O ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 DIMETHICONE INACTIVE INGREDIENT 92RU3N3Y1O ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) INACTIVE INGREDIENT ZYD53NBL45 ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) INACTIVE INGREDIENT ZYD53NBL45 ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 SACCHARIN SODIUM DIHYDRATE INACTIVE INGREDIENT SB8ZUX40TY ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 SACCHARIN SODIUM DIHYDRATE INACTIVE INGREDIENT SB8ZUX40TY ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0536-0091 ALUMINUM HYDROXIDE LIQUID [RUGBY LABORATORIES] 3 Current NDC, Legacy NDC, 1 package rows 20231103_27c574a5-1fe0-4973-9a31-9beb4fc6ec46.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 0536-0091-85 00536009185 473 mL in 1 BOTTLE (0536-0091-85) 473 ml 2017-07-01 0000-00-00 No No Current