CETIRIZINE HYDROCHLORIDE- cetirizine hydrochloride tablets tablet, film coated 
Bryant Ranch Prepack

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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:

.

Warnings

Ask a doctor before use if you have

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

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

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

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

Inactive ingredients

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

Questions?

call 1-888-375-3784.

HOW SUPPLIED

NDC: 71335-9612-1: 30 Tablets in a BOTTLE

NDC: 71335-9612-2: 14 Tablets in a BOTTLE

NDC: 71335-9612-3: 7 Tablets in a BOTTLE

NDC: 71335-9612-4: 10 Tablets in a BOTTLE

NDC: 71335-9612-5: 15 Tablets in a BOTTLE

NDC: 71335-9612-6: 90 Tablets in a BOTTLE

NDC: 71335-9612-7: 20 Tablets in a BOTTLE

NDC: 71335-9612-8: 60 Tablets in a BOTTLE

NDC: 71335-9612-9: 100 Tablets in a BOTTLE

Cetirizine Hcl 10mg Tablet

Label
CETIRIZINE HYDROCHLORIDE 
cetirizine hydrochloride tablets tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-9612(NDC:43598-811)
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
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
STARCH, CORN (UNII: O8232NY3SJ)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize7mm
FlavorImprint Code C
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71335-9612-130 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
2NDC:71335-9612-214 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
3NDC:71335-9612-37 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
4NDC:71335-9612-410 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
5NDC:71335-9612-515 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
6NDC:71335-9612-690 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
7NDC:71335-9612-720 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
8NDC:71335-9612-860 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
9NDC:71335-9612-9100 in 1 BOTTLE; Type 0: Not a Combination Product01/03/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07834312/17/2018
Labeler - Bryant Ranch Prepack (171714327)
Registrant - Bryant Ranch Prepack (171714327)
Establishment
NameAddressID/FEIBusiness Operations
Bryant Ranch Prepack171714327REPACK(71335-9612) , RELABEL(71335-9612)

Revised: 1/2023
Document Id: 5c400abf-9305-4291-9226-d1b605b4fc38
Set id: e4324124-13f8-4450-9fd6-686bd6e25578
Version: 100
Effective Time: 20230103
 
Bryant Ranch Prepack