ALL DAY ALLERGY- cetirizine hydrochloride tablet, film coated 
Kroger Company

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Kroger Co. All Day Allergy 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

Other information

store between 20-25°C (68-77°F)
do not use if printed foil under cap is broken or missing

Inactive ingredients

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

Questions or comments?

1-800-632-6900

Principal Display Panel

COMPARE TO the active ingredient of ZYRTEC®

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OUR PHARMACIST RECOMMENDED

ORIGINAL PRESCRIPTION STRENGTH

All Day Allergy

Cetirizine Hydrochloride Tablets, 10 mg

Antihistamine

INDOOR & OUTDOOR ALLERGIES

24 HOUR

24 HOUR RELIEF OF:

Sneezing; Runny Nose; Itchy, Watery Eyes; Itchy Throat or Nose

actual size

70 TABLETS

all day allergy image
ALL DAY ALLERGY 
cetirizine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-458
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)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize10mm
FlavorImprint Code 4H2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-458-6614 in 1 CARTON01/08/2008
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:30142-458-391 in 1 CARTON09/13/2008
230 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:30142-458-951 in 1 CARTON09/24/200808/01/2019
345 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:30142-458-761 in 1 CARTON09/02/200806/01/2019
4120 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:30142-458-481 in 1 CARTON08/10/201105/19/2019
5180 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:30142-458-491 in 1 CARTON04/03/2014
640 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:30142-458-061 in 1 CARTON10/02/2017
770 in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:30142-458-721 in 1 CARTON09/02/200805/08/2019
860 in 1 BOTTLE; Type 0: Not a Combination Product
9NDC:30142-458-922 in 1 CARTON01/15/2018
970 in 1 BOTTLE; Type 0: Not a Combination Product
10NDC:30142-458-881 in 1 CARTON04/19/2018
10365 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07833601/08/2008
Labeler - Kroger Company (006999528)

Revised: 9/2020
Document Id: c5a9ba6f-317d-4652-b0b2-3bcd867060f2
Set id: d548cf8d-e9e9-4201-89de-c5039b70414b
Version: 8
Effective Time: 20200924
 
Kroger Company