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Equaline All Day Allergy Prescribing Information

Package insert / product label
Generic name: cetirizine hydrochloride
Dosage form: tablet
Drug class: Antihistamines

Medically reviewed by Drugs.com. Last updated on Aug 4, 2023.

Active ingredient (in each tablet)

Cetirizine HCl 10 mg

Purpose

Antihistamine

Indications and Usage for Equaline All Day Allergy

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)

Equaline All Day Allergy Dosage and Administration

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

Storage and Handling

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?

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compare to Zyrtec® active ingredient

EQUALINE®

all day allergy

cetirizine hydrochloride tablets, 10mg (antihistamine)

indoor & outdoor allergies

24 hour relief of:

sneezing

runny nose

itchy, watery eyes

itchy throat or nose

actual size

30 tablets

ORIGINAL PRESCRIPTION STRENGTH

4h2-el-all-day-allergy
EQUALINE ALL DAY ALLERGY
cetirizine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-458
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 Code4H2
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-458-391 in 1 PACKAGE11/03/2008
130 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:41163-458-6614 in 1 CARTON01/23/2008
21 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:41163-458-721 in 1 CARTON09/09/2009
360 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:41163-458-761 in 1 CARTON08/05/200911/30/2021
4120 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:41163-458-951 in 1 PACKAGE10/07/200803/01/2020
545 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:41163-458-581 in 1 CARTON11/21/201912/31/2021
640 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07833601/23/2008
Labeler - United Natural Foods, Inc. dba UNFI (943556183)

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