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Cetirizine by Bryant Ranch Prepack

Medically reviewed on July 17, 2018

Dosage form: tablet
Labeler: Bryant Ranch Prepack
NDC Code: 63629-3708

Cetirizine Tablet

Active ingredient (in each tablet)

Cetirizine HCl 10 mg




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


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.

6 years and over

adults and children

one 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
  • do not use if blister unit is broken or torn (Blister Only)
  • store between 20° to 25°C (68° to 77°F)

Inactive ingredients

corn starch, FD&C blue no. 1, hypromellose, lactose, magnesium stearate, polydextrose, polyethylene glycol, povidone, titanium dioxide, triacetin

Cetirizine 10mg Tablet
cetirizine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63629-3708(NDC:45802-919)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Product Characteristics
ColorWHITEScoreno score
FlavorImprint Code4H2
#Item CodePackage Description
1NDC:63629-3708-130 TABLET in 1 BOTTLE
2NDC:63629-3708-214 TABLET in 1 BOTTLE
3NDC:63629-3708-37 TABLET in 1 BOTTLE
4NDC:63629-3708-410 TABLET in 1 BOTTLE
5NDC:63629-3708-515 TABLET in 1 BOTTLE
6NDC:63629-3708-690 TABLET in 1 BOTTLE
7NDC:63629-3708-720 TABLET in 1 BOTTLE
8NDC:63629-3708-860 TABLET in 1 BOTTLE
9NDC:63629-3708-9100 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Labeler - Bryant Ranch Prepack (171714327)
Registrant - Bryant Ranch Prepack (171714327)
Bryant Ranch Prepack171714327REPACK(63629-3708), RELABEL(63629-3708)

Bryant Ranch Prepack

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.