ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated 
Gobrands, Inc

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Allergy Relief

Drug Facts

Active Ingredient (in each tablet)

Cetirizine HCl 10 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
• runny nose • itchy, watery eyes • sneezing • itching of the nose or throat

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.

When using this product
• drowsiness may occur • avoid alcoholic drinks • alcohol, sedatives, and tranquilizers may increase drowsiness • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding, • if breast-feeding: not recommended • if pregnant: ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

Directions

adults & children 6 years & overone 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg
product may be appropriate for less severe symptoms
adults 65 years & overask a doctor
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information

• store between 20–25°C (68–77°F)

Inactive ingredients

Lactose, povidone, maize starch, magnesium stearate, purified water, titanium dioxide, hypromellose, macrogol

Questions or comments?

1-888-333-9792

PRINCIPAL DISPLAY PANEL

Cetirizine Label

Cetirizine Carton

ALLERGY RELIEF 
cetirizine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82501-1574
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
POVIDONE (UNII: FZ989GH94E)  
STARCH, CORN (UNII: O8232NY3SJ)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
Product Characteristics
ColorwhiteScoreno score
ShapeSQUARESize8mm
FlavorImprint Code CTN10
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82501-1574-31 in 1 CARTON05/27/2022
130 in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07782905/27/2022
Labeler - Gobrands, Inc (057499049)

Revised: 12/2023
Document Id: 0c046516-3ae9-25e6-e063-6394a90a2ea9
Set id: b079e2e5-8e4b-4419-bfe5-2315c861a5d1
Version: 4
Effective Time: 20231208
 
Gobrands, Inc