ALLERGY RELIEF- cetirizine hydrochloride tablet, coated 
CHAIN DRUG MARKETING ASSOCIATION, INC.

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1194A-QCH-2024-0816

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:

Warnings

Do not useif 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 haveliver or kidney disease.  Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you aretaking 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 and children 6 years and 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 and overask a doctor
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide.

PRINCIPAL DISPLAY PANEL

QUALITY CHOICE®

NDC 83324-091-14

†Compare to Active ingredient in ZYRTEC® Allergy 

Original Prescription Strength

Allergy Relief 

24 Hour

Cetirizine Hydrochloride Tablets, 10 mg

Antihistamine

Indoor & Outdoor Allergies

For Relief of: Sneezing | Runny Nose | Itchy, Watery Eyes | Itchy Throat or Nose

Actual Size

14 TABLETS

image description

ALLERGY RELIEF 
cetirizine hydrochloride tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-091
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
Product Characteristics
Colorwhite (white to off white) Score2 pieces
ShapeRECTANGLE (rounded off rectangualr) Size9mm
FlavorImprint Code G;4
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-091-141 in 1 CARTON08/16/2024
114 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:83324-091-301 in 1 CARTON08/16/2024
230 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:83324-091-901 in 1 CARTON08/17/2024
390 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20927408/16/2024
Labeler - CHAIN DRUG MARKETING ASSOCIATION, INC. (011920774)

Revised: 8/2024
Document Id: 1fd10ca6-5ab4-50d2-e063-6294a90a3a09
Set id: 6eb22b5a-ff30-44f8-aca2-3f73614515a8
Version: 2
Effective Time: 20240816
 
CHAIN DRUG MARKETING ASSOCIATION, INC.