UP AND UP ALL DAY ALLERGY RELIEF- cetirizine hydrochloride tablet 
Target Corporation

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Target Corporation All Day Allergy Relief 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 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. (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

Inactive ingredients

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

Questions?

Call 1-800-910-6874

Principal Display Panel

all day allergy relief

cetirizine hydrochloride tablets, 10 mg

antihistamine

Compare to active ingredient in Zyrtec®

original prescription strength

indoor and outdoor allergies

24 hour relief of: sneezing/runny nose/itchy, watery eyes/itchy throat or nose

ACTUAL SIZE

# TABLETS {Replace "#" with the number of Tablets in the package}

All Day Allergy Relief Carton Image
UP AND UP ALL DAY ALLERGY RELIEF 
cetirizine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-458
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
STARCH, CORN (UNII: O8232NY3SJ)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
POVIDONES (UNII: FZ989GH94E)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize10mm
FlavorImprint Code 4H2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-458-661 in 1 CARTON05/27/200910/01/2016
114 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:11673-458-391 in 1 PACKAGE05/27/200910/01/2016
230 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:11673-458-951 in 1 PACKAGE05/27/200910/01/2016
345 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:11673-458-761 in 1 PACKAGE05/27/200910/01/2016
4120 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:11673-458-481 in 1 PACKAGE05/27/200910/01/2016
5180 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:11673-458-061 in 1 PACKAGE05/27/200910/01/2016
670 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:11673-458-721 in 1 PACKAGE05/27/200910/01/2016
760 in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:11673-458-741 in 1 CARTON05/27/200910/01/2016
814 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07833605/27/200910/01/2016
Labeler - Target Corporation (006961700)

Revised: 11/2017
 
Target Corporation