Skip to Content

← See all Cetirizine Hydrochloride brands

Cetirizine Hydrochloride by Dr.Reddy's Laboratories Limited

Medically reviewed on October 2, 2017

Dosage form: tablet, film coated
Ingredients: CETIRIZINE HYDROCHLORIDE 10mg
Labeler: Dr.Reddy's Laboratories Limited
NDC Code: 55111-351

Cetirizine Hydrochloride Tablets

Drug Facts

Active ingredient (in each tablet)

Cetirizine HCl, 10mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose
  • sneezing
  • itchy, watery eyes
  • 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 antihistaminecontaining 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.

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
  • store between 20° to 25°C (68° to 77°F)

Inactive ingredients

hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, povidone, starch, titanium dioxide.

Questions?

call 1-888-375-3784.

PRINCIPAL DISPLAY PANEL - Container Labeling

10 mg Container Labeling

PRINCIPAL DISPLAY PANEL - Containers

10 mg Containers:

    

    

CETIRIZINE HYDROCHLORIDE 
cetirizine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55111-351
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (CETIRIZINE) CETIRIZINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES 
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
POLYETHYLENE GLYCOL 400 
POVIDONE 
STARCH, CORN 
TITANIUM DIOXIDE 
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize6mm
FlavorImprint CodeRDY;351
Contains    
Packaging
#Item CodePackage Description
1NDC:55111-351-301 BOTTLE (1 BOTTLE) in 1 CARTON
130 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
2NDC:55111-351-451 BOTTLE (1 BOTTLE) in 1 CARTON
245 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
3NDC:55111-351-601 BOTTLE (1 BOTTLE) in 1 CARTON
360 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
4NDC:55111-351-901 BOTTLE (1 BOTTLE) in 1 CARTON
490 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
5NDC:55111-351-041 BOTTLE (1 BOTTLE) in 1 CARTON
5120 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
6NDC:55111-351-472 BOTTLE (1 BOTTLE) in 1 CARTON
6175 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
7NDC:55111-351-511 BOTTLE (1 BOTTLE) in 1 CARTON
775 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
8NDC:55111-351-742 BLISTER PACK (TABLET) in 1 CARTON
87 TABLET, FILM COATED (TABLET) in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07834301/15/2008
CETIRIZINE HYDROCHLORIDE 
cetirizine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55111-699
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (CETIRIZINE) CETIRIZINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES 
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
POLYETHYLENE GLYCOL 400 
POVIDONE 
STARCH, CORN 
TITANIUM DIOXIDE 
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize7mm
FlavorImprint CodeC
Contains    
Packaging
#Item CodePackage Description
1NDC:55111-699-901 BOTTLE (1 BOTTLE) in 1 CARTON
190 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
2NDC:55111-699-451 BOTTLE (1 BOTTLE) in 1 CARTON
245 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
3NDC:55111-699-301 BOTTLE (1 BOTTLE) in 1 CARTON
330 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
4NDC:55111-699-511 BOTTLE (1 BOTTLE) in 1 CARTON
475 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
5NDC:55111-699-041 BOTTLE (1 BOTTLE) in 1 CARTON
5120 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
6NDC:55111-699-191 BOTTLE (1 BOTTLE) in 1 CARTON
6175 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
7NDC:55111-699-472 BOTTLE (1 BOTTLE) in 1 CARTON
7175 TABLET, FILM COATED (1 TABLET) in 1 BOTTLE
8NDC:55111-699-601 BOTTLE (1 BOTTLE) in 1 CARTON
860 TABLET, FILM COATED (TABLET) in 1 BOTTLE
9NDC:55111-699-731 BOTTLE (1 BOTTLE) in 1 CARTON
9365 TABLET, FILM COATED (TABLET) in 1 BOTTLE
10NDC:55111-699-742 BLISTER PACK (1 BLISTER PACK) in 1 CARTON
107 TABLET, FILM COATED (1 TABLET) in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07834301/15/2008
Labeler - Dr.Reddy's Laboratories Limited (650562841)

 
Dr.Reddy's Laboratories Limited

← See all Cetirizine Hydrochloride brands

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide