CETIRIZINE HYDROCHLORIDE (ALLERGY)- cetirizine hydrochloride tablet

Cetirizine Hydrochloride (Allergy) by

Drug Labeling and Warnings

Cetirizine Hydrochloride (Allergy) by is a Otc medication manufactured, distributed, or labeled by Proficient Rx LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each tablet)

For 10 mg:

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]

Directions

For 5 mg:

• adults and children 6 years and over:

  1 to 2 tablets once daily depending upon severity of symptoms; do not take more than 2 tablets in 24 hours.;

• adults 65 years and over:

  1 tablet once a day; do not take more than 1 tablet in 24 hours;

• children under 6 years of age:

  ask a doctor;

• consumers with liver or kidney disease:

  ask a doctor;

For 10 mg:

• 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)
• TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING.

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide.

Questions?

call 1-855-274-4122

Distributed by:
AUROHEALTH LLC
2572 Brunswick Pike
Lawrenceville, NJ 08648

Made in India

Repackaged by:
Proficient Rx LP
Thousand Oaks, CA 91320

Code: TS/DRUGS/19/19

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (10's Tablet Container Carton Label)

NDC: 71205-700-10
*Compare to the active
ingredient of Zyrtec®

Allergy Relief
Cetirizine Hydrochloride Tablets USP 10 mg
Antihistamine
Original Prescription Strength

Indoor & Outdoor Allergies
24 Hour Relief of :

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

10 Tablets
10 mg each

INGREDIENTS AND APPEARANCE

CETIRIZINE HYDROCHLORIDE (ALLERGY) 
cetirizine hydrochloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71205-700(NDC:58602-445)
Route of Administration	ORAL

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

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE (White to Off-white)	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code	X;36
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71205-700-06	6 in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2024
2	NDC: 71205-700-10	10 in 1 BOTTLE; Type 0: Not a Combination Product	10/20/2022
3	NDC: 71205-700-12	12 in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2024
4	NDC: 71205-700-14	14 in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2024
5	NDC: 71205-700-15	15 in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2024
6	NDC: 71205-700-20	20 in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2024
7	NDC: 71205-700-21	21 in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2024
8	NDC: 71205-700-30	30 in 1 BOTTLE; Type 0: Not a Combination Product	09/16/2022
9	NDC: 71205-700-60	60 in 1 BOTTLE; Type 0: Not a Combination Product	09/16/2022
10	NDC: 71205-700-90	90 in 1 BOTTLE; Type 0: Not a Combination Product	09/16/2022
11	NDC: 71205-700-00	100 in 1 BOTTLE; Type 0: Not a Combination Product	03/08/2024
12	NDC: 71205-700-72	120 in 1 BOTTLE; Type 0: Not a Combination Product	03/08/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA090760	08/05/2015

Labeler - Proficient Rx LP (079196022)

Establishment
Name	Address	ID/FEI	Business Operations
Proficient Rx LP		079196022	REPACK(71205-700) , RELABEL(71205-700)