ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated 
Strategic Sourcing Services LLC

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Allergy Relief (Cetirizine HCl Tablets)

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:
● runny nose
● sneezing
● itchy, watery eyes
● itching of the nose or throat

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 ifan 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 over:  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
store between 20° to 25°C (68° to 77°F)

Inactive ingredients
colloidal silicon dioxide**, croscarmellose sodium**, hypromellose, lactose, magnesium stearate, maize starch**, microcrystalline cellulose**, polyethylene glycol, povidone**, titanium dioxide
**containes one or more of these ingrdients

Questions or comments?

833-358-6431

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ALLERGY RELIEF 
cetirizine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70677-1241
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE10 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MAIZE INVERT SUGAR (UNII: ED959S6ACY)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Colorwhite (white to off-white) Scoreno score
ShapeBULLET (barrel shaped, biconvex) Size8mm
FlavorImprint Code CTN;10
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70677-1241-1120 in 1 BOTTLE; Type 0: Not a Combination Product01/24/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07782901/23/2024
Labeler - Strategic Sourcing Services LLC (116956644)

Revised: 2/2024
Document Id: 10bc5029-5cad-3575-e063-6394a90a2209
Set id: 54509525-ad99-4165-a571-47ece058e292
Version: 2
Effective Time: 20240206
 
Strategic Sourcing Services LLC