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 17 of 34 · 678 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ultra Strength CALCIUM CARBONATE BETTER LIVING BRANDS LLC 3ff92c9a-987f-468e-9e18-1e3e171ede14 2025-10-29 Warnings Exact identifier application number: M001 Ultra Strength CALCIUM CARBONATE BETTER LIVING BRANDS LLC 35b3d9d0-b04d-4f6d-b99d-435233803d4b 2025-10-29 Warnings Exact identifier application number: M001 Ultra Strength ANTACID TABLETS SAFEWAY 4c6cdd81-5145-4a1f-888f-85cf5d856c39 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength Smooth ANTACID TABLETS SAFEWAY 8ed35c3b-9878-4889-90f7-a3973cf806e0 2025-10-29 Warnings Exact identifier application number: M001 Publix Regular Strength Assorted Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC fd637431-7a08-4454-9cae-a68716d2d0fa 2025-10-28 Warnings Exact identifier application number: M001 Publix Regular Strength Peppermint Flavor CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC c41b6cc2-c852-45fd-858c-c7bedc5dc882 2025-10-28 Warnings Exact identifier application number: M001 Publix Extra Strength Assorted Berry CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC a270fc36-f2b2-4f56-81d4-cf165f6b5abe 2025-10-28 Warnings Exact identifier application number: M001 Extra Strength Sugar Free Orange Cream Flavor CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 4dbdabc4-280d-4c9a-8c54-84afc615c8c7 2025-10-28 Warnings Exact identifier application number: M001 Publix Extra Strength Tropical Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 28e8dd03-25cf-43db-8c4d-3aae99be9d53 2025-10-28 Warnings Exact identifier application number: M001 Publix Ultra Strength Assorted Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 9e1c883f-016e-4c05-b27a-750d14c0f3e5 2025-10-28 Warnings Exact identifier application number: M001 Ultra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc., 48827658-02f7-4599-a90a-1543b30b9de1 2025-10-27 Warnings Exact identifier application number: M001 Regular Strength Antacid ANTACID Wal-Mart Stores,Inc., 6e7cd170-b169-4fc0-bc90-f4421bbd9fcd 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc., febe9d70-9a1f-43a9-8ad0-3134eefc6967 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc., d399f927-e80b-4162-a1f1-ef6159d6f7b1 2025-10-27 Warnings Exact identifier application number: M001 equate Sugar Free Extra Strength Antacid Orange Cream Flavor ANTACID Wal-Mart Stores,Inc., 53a22b37-66af-4735-b262-15e06ad7bf76 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc. 841ddf88-a016-4a3c-9508-5d5702883d8f 2025-10-27 Warnings Exact identifier application number: M001 Ultra Strength Antacid Assorted Fruit CALCIUM CARBONATE Wal-Mart Stores,Inc., 6900fabc-2299-48cf-bbda-c92649cfd0e1 2025-10-27 Warnings Exact identifier application number: M001 equate Ultra Strength Antacid Peppermint Flavor ANTACID TABLETS Wal-Mart Stores,Inc., 6a18cd92-cc51-401b-9074-fbaa1afb42ac 2025-10-27 Warnings Exact identifier application number: M001 Extra Strength Smooth Antacid ANTACID TABLETS Wal-Mart Stores,Inc., 9acdfb08-043d-48a5-95f9-54bcba733c6e 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE Wal-Mart Stores,Inc 448d1c72-2308-4041-8ba6-dd1e0802cc47 2025-10-27 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 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