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Cetirizine hydrochloride 10 mg - Medication Information

Product NDC Code 73581-202
Drug Name

Cetirizine hydrochloride 10 mg

Type Brand
Pharm Class Histamine H1 Receptor Antagonists [MoA],
Histamine-1 Receptor Antagonist [EPC]
Active Ingredients
Cetirizine hydrochloride 10 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 1014678
Application Number ANDA209274
Labeler Name YYBA CORP
Packages
Package NDC Code Description
73581-202-01 100 tablet in 1 bottle (73581-202-01)
73581-202-05 500 tablet in 1 bottle (73581-202-05)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each tablet) Cetirizine Hydrochloride 10 mg Purpose Antihistamine

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions adults and children 6 years and over take one 10 mg tablet oncedaily; do not take more than one 10mg tablet in 24 hours. A 5mg product may be appropriate for less severe symptoms. adults 65 years and older ask a doctor children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor
adults and children 6 years and overtake one 10 mg tablet oncedaily; do not take more than one 10mg tablet in 24 hours. A 5mg product may be appropriate for less severe symptoms.
adults 65 years and olderask a doctor
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
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

Purpose

Information about the drug product’s indications for use.
Purpose Antihistamine

Spl product data elements

Usually a list of ingredients in a drug product.
CETIRIZINE HYDROCHLORIDE 10 MG CETIRIZINE HYDROCHLORIDE SILICON DIOXIDE CROSCARMELLOSE SODIUM HYPROMELLOSE 2208 (100 MPA.S) LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 1000 TITANIUM DIOXIDE CETIRIZINE HYDROCHLORIDE CETIRIZINE G4

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
01b LBL_Cetrizine Hydrochloride_10mg 01b DF1_Cetrizine Hydrochloride_10mg 01b DF2_Cetrizine Hydrochloride_10mg

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
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)

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information store between 20° and 25°C (68° and 77°F)

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? call toll-free 1-866-933-6337

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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 hydroxyine. 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

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API