ALLERGY RELIEF- cetirizine hcl tablet 
Bryant Ranch Prepack

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Drug Facts

Active ingredient (in each tablet)

Cetirizine HCl 10 mg

Purpose

Antihistamine

Uses

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
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • 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 (1-800-222-1222) right away.

Directions

adults and children 6 years and over Take 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 over ask a doctor
children under 6 years of age ask a doctor
consumers with liver or kidney disease ask a doctor

Other Information

Inactive ingredients

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

Questions or comments?

Call  1-888-588-1418 Monday-Friday 9AM-5PM EST

Principal Display Panel

*Compare to the active ingredient in Zyrtec®

Allergy Relief

Cetirizine HCl Tablets USP, 10 mg/Antihistamine

Indoor & Outdoor Allergies

24 hour relief of

Original Prescription Strength

Tablets

*This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Zyrtec®.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

Distributed by:

Camber Consumer Care Inc, Piscataway, NJ 08854, USA

HOW SUPPLIED

Cetirizine Hydrochloride 10 mg Tablet

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

Cetirizine Hydrochloride 10 mg Tablet

Label
ALLERGY RELIEF 
cetirizine hcl tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-9733(NDC:69230-304)
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)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
Product Characteristics
ColorwhiteScore2 pieces
ShapeOVALSize9mm
FlavorImprint Code G;4
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71335-9733-130 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/05/2023
2NDC:71335-9733-214 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/27/2023
3NDC:71335-9733-37 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/05/2024
4NDC:71335-9733-410 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/05/2024
5NDC:71335-9733-515 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/05/2024
6NDC:71335-9733-690 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/05/2024
7NDC:71335-9733-720 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/05/2024
8NDC:71335-9733-860 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/05/2024
9NDC:71335-9733-9100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/25/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20927412/31/201812/31/2024
Labeler - Bryant Ranch Prepack (171714327)
Registrant - Bryant Ranch Prepack (171714327)
Establishment
NameAddressID/FEIBusiness Operations
Bryant Ranch Prepack171714327REPACK(71335-9733) , RELABEL(71335-9733)

Revised: 4/2024
Document Id: 7e4a2d02-c2b3-4a1f-8373-a0b0dec5ddea
Set id: 7e4a2d02-c2b3-4a1f-8373-a0b0dec5ddea
Version: 102
Effective Time: 20240405
 
Bryant Ranch Prepack