ALUMINUM HYDROXIDE - aluminum hydroxide liquid 
ATLANTIC BIOLOGICALS CORP.

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Active ingredient (in each 5 mL teaspoonful)

Aluminum hydroxide 320 mg

Purpose

Antacid



Uses

relieves


Warnings

taking a prescription drug. Antacids may interact with certain prescription drugs. you may get constipated symptoms last more than 2 weeks

Ask a doctor or pharmacist before use if you are

When using this product


Stop use and ask a doctor if

Keep out of reach of children.

Directions

• shake well before using • do not take more than 12 teaspoonfuls in 24 hours • do not use the maximum dosage for more than 2 weeks • 2 teaspoonfuls 5-6 times daily after meals and at bedtime followed by a sip of water if needed




dosage:

Other information

• store at room temperature • protect from freezing  • keep tightly closed •


TAMPER-EVIDENT: DO NOT USE IF FOIL SEAL UNDER CAP IS BROKEN OR MISSING.

Inactive ingredients

benzyl alcohol, butylparaben, flavor, glycerin, hydroxyethylcellulose, propylparaben, purified water, saccharin sodium, simethicone emulsion, sorbitol solution

Questions or comments?

Call 9am - 5pm EST, Monday-Friday 1-800-645-2158

DISTRIBUTED BY:

ATLANTIC BIOLOGICALS CORP.

MIAMI, FL 33179

ALUMINUM HYDROXIDE LIQUID

image description

ALUMINUM HYDROXIDE  
aluminum hydroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17856-0091(NDC:0536-0091)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE320 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINT (mint) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17856-0091-330 mL in 1 CUP; Type 0: Not a Combination Product04/16/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02/01/2005
Labeler - ATLANTIC BIOLOGICALS CORP. (047437707)
Registrant - ATLANTIC BIOLOGICALS CORP. (047437707)
Establishment
NameAddressID/FEIBusiness Operations
UNIT DOSE SOLUTIONS360804194REPACK(17856-0091)

Revised: 4/2024
Document Id: 86d6de98-4061-43d2-acaf-07cae8f5bf87
Set id: 60a54d4e-89c2-4329-86bf-a288527f37b5
Version: 5
Effective Time: 20240416
 
ATLANTIC BIOLOGICALS CORP.