Drugplain

Cetirizine Hydrochloride 10 mg/1

Cetirizine Hydrochloride · TABLET · FAMILY DOLLAR SERVICES, INC

10 Recalls on Record
Plain English

Cetirizine hydrochloride is an antihistamine tablet taken by mouth that helps relieve allergy symptoms such as sneezing, itching, watery eyes, and runny nose. This medication is available over-the-counter without a prescription.

Key Facts

Brand Name
Cetirizine Hydrochloride
Generic Name
Cetirizine Hydrochloride
NDC Code (Product)
55319-939
Manufacturer
FAMILY DOLLAR SERVICES, INC
Strength
10 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA077498
Marketing Start
09/01/2017

Recall History

10 Recalls on Record
Class II03/13/2025

Glenmark Pharmaceuticals Inc., USA

CGMP Deviations

OngoingVoluntary: Firm initiated
Class III04/09/2014

Caraco Pharmaceutical Laboratories, Ltd.

Failed Impurities/Degradation Specifications: out of specification results for impurities/degradation testing for N-Oxide

TerminatedVoluntary: Firm initiated
Class III04/09/2014

Caraco Pharmaceutical Laboratories, Ltd.

Failed Impurities/Degradation Specifications: out of specification results for impurities/degradation testing for N-Oxide

TerminatedVoluntary: Firm initiated
Class II10/19/2018

Taro Pharmaceuticals U.S.A., Inc.

Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.

TerminatedVoluntary: Firm initiated
Class III09/12/2025

JB Chemicals and Pharmaceuticals Ltd

Tablet/Capsules Imprinted with Wrong ID

OngoingVoluntary: Firm initiated
Class II05/21/2019

Torrent Pharma Inc

cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).

TerminatedVoluntary: Firm initiated
Class II10/19/2018

Taro Pharmaceuticals U.S.A., Inc.

Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.

TerminatedVoluntary: Firm initiated
Class II10/19/2018

Taro Pharmaceuticals U.S.A., Inc.

Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.

TerminatedVoluntary: Firm initiated
Class II05/21/2019

Torrent Pharma Inc

cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).

TerminatedVoluntary: Firm initiated
Class III12/16/2013

Qualitest Pharmaceuticals

Failed impurities/degradation specifications; out of specification for the known impurity 4-chlorobenzophenone.

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective13,340 reports
fatigue13,152 reports
pain12,345 reports
rash10,013 reports
off label use9,670 reports
abdominal discomfort9,473 reports
alopecia9,378 reports
rheumatoid arthritis8,831 reports
systemic lupus erythematosus8,599 reports
pemphigus8,400 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat

Dosage & Administration

Directions use only with enclosed dosing cup find right dose on chart below mL = milliliter adults and children 6 years and over 5 mL or 10 mL once daily depending upon severity of symptoms; do not take more than 10 mL in 24 hours.. adults 65 years and older 5 mL once daily; do not take more than 5 mL in 24 hours children 2 to under 6 years of age 2.5 mL once daily. If needed, dose can be increased to a maximum of 5 mL once daily or 2.5 mL every 12 hours. Do not give more than 5 mL in 24 hours. children under 2 years of age ask a doctor consumers with liver or kidney disease ask a doctor

Warnings

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).

Frequently Asked Questions

What is Cetirizine Hydrochloride used for?

Cetirizine hydrochloride is an antihistamine tablet taken by mouth that helps relieve allergy symptoms such as sneezing, itching, watery eyes, and runny nose. This medication is available over-the-counter without a prescription.

Is Cetirizine Hydrochloride a controlled substance?

Cetirizine Hydrochloride is not classified as a controlled substance by the DEA.

What is the generic name for Cetirizine Hydrochloride?

The generic name for Cetirizine Hydrochloride is Cetirizine Hydrochloride. There are 11 other brand versions of Cetirizine Hydrochloride.

What is the NDC code for Cetirizine Hydrochloride 10 mg/1?

The NDC (National Drug Code) for Cetirizine Hydrochloride 10 mg/1 is 55319-939, listed by FAMILY DOLLAR SERVICES, INC.