CETIRIZINE HYDROCHLORIDE tablet, chewable

SPL UNCLASSIFIED SECTION

Drug Facts
Active ingredient (in each chewable tablet)

Cetirizine hydrochloride, USP 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)

adults and children 6 years and over	Chew and swallow 1 tablet (10 mg) once daily; do not take more than 1 tablet (10 mg) 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)
- do not use if inner safety seal is open or torn
- see side panel for lot number and expiration date
Inactive ingredients

acesulfame potassium, colloidal silicon dioxide, compressible sugar, crospovidone, FD & C Blue No # 2 Aluminum Lake, FD & C Red No # 40 Aluminum Lake, guar gum, magnesium oxide light powder, magnesium stearate, mannitol, microcrystalline cellulose, pregelatinized starch, prosweet N & A flavor powder, talc, tutti frutti flavor
Questions?

Call toll free 1-800-818-4555 weekdays
SPL UNCLASSIFIED SECTION

Distributed by:
Ohm Laboratories Inc.
New Brunswick, NJ 08901
PRINCIPAL DISPLAY PANEL - 10 mg Tablet Bottle Carton
†Compare To
the active ingredient of
Children's Zyrtec®

NDC: 51660-066-30

ohm®

Original Prescription Strength

Cetirizine
Hydrochloride
Chewable
Tablets 10 mg

Antihistamine

Allergy

Tutti-frutti Flavor
No Water Needed

Indoor + Outdoor Allergies

Actual Size

24 Hour Relief of:
- Sneezing
- Itchy, Watery Eyes
- Runny Nose
- Itchy Throat or Nose
30 CHEWABLE
TABLETS

CETIRIZINE HYDROCHLORIDE
cetirizine hydrochloride tablet, chewable

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24)	CETIRIZINE HYDROCHLORIDE	10 mg

Ingredient Name	Strength
Inactive Ingredients
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SUCROSE (UNII: C151H8M554)
CROSPOVIDONE (120 .MU.M) (UNII: 68401960MK)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GUAR GUM (UNII: E89I1637KE)
MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
STARCH, CORN (UNII: O8232NY3SJ)
TALC (UNII: 7SEV7J4R1U)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC: 51660-066-30	1 in 1 CARTON	07/21/2022
1		30 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA090142	07/21/2022

Labeler - OHM LABORATORIES INC. (184769029)

Name	Address	ID/FEI	Business Operations
Establishment
Sun Pharmaceutical Industries Limited		725959238	MANUFACTURE(51660-066)

Cetirizine Hydrochloride by