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Allergy - Medication Information

Product NDC Code 41226-692
Drug Name

Allergy

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, FILM COATED
RxCUI drug identifier 1014678
Application Number ANDA078933
Labeler Name Kroger Company
Packages
Package NDC Code Description
41226-692-14 2 bottle in 1 carton (41226-692-14) / 70 tablet, film coated in 1 bottle
41226-692-65 1 bottle in 1 carton (41226-692-65) / 365 tablet, film coated in 1 bottle
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Cetirizine HCl 10 mg

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: 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

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients corn starch, hypromellose, lactose monohydrate, magnesium stearate, 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.
Antihistamine

Spl product data elements

Usually a list of ingredients in a drug product.
ALLERGY CETIRIZINE HYDROCHLORIDE STARCH, CORN LACTOSE MONOHYDRATE POVIDONE POLYETHYLENE GLYCOL, UNSPECIFIED HYPROMELLOSES MAGNESIUM STEARATE TITANIUM DIOXIDE CETIRIZINE HYDROCHLORIDE CETIRIZINE Rounded-off rectangular shaped (white to off white) J;220

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.
Cetirizine Hydrochloride Tablets 10mg-70ct-Carton Cetirizine Hydrochloride Tablets 10mg-365ct-Carton Cetirizine Hydrochloride Tablets 10mg-365ct-Bottle label Cetirizine Hydrochloride tablets 10mg-70ct-Bottle label

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
DRUG FACTS OTHER INFORMATION Other information store between 20° to 25°C (68°to 77°F)

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

Ask doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.

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).

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-800-632-6900

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
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

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding: if breast-feeding: not recommended if pregnant: ask a health professional before use.

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 hydroxyzine.

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