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CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

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Compare CHILDREN'S ZYRTEC HIVES RELIEF SYRUP to:

Generic Name for CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

Cetirizine HCl 1mg/mL; grape flavor.

Legal Classification:

OTC

Pharmacological Class for CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

Antihistamine.

Manufacturer of CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

McNeil Consumer & Specialty Pharmaceuticals

Indications for CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

Itching due to urticaria.

Adults and Children:

<6years: not recommended. ≥6years: initially 5–10mg once daily. ≥65years: use syrup: 5mg once daily. Hepatic or renal impairment: individualize.

Also:

CHILDREN'S ZYRTEC ALLERGY SYRUP

CHILDREN'S ZYRTEC CHEWABLE

CHILDREN'S ZYRTEC PERFECT MEASURE

ZYRTEC

ZYRTEC HIVES RELIEF

ZYRTEC LIQUID GELS

Contraindications for CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

Hydroxyzine sensitivity.

Warnings/Precautions for CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

Hives Relief: not used for prevention or as a substitute for epinephrine. Hepatic or renal dysfunction. Pregnancy. Nursing mothers: not recommended.

Interactions for CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

Potentiates CNS depression with alcohol, other CNS depressants.

Adverse Reactions for CHILDREN'S ZYRTEC HIVES RELIEF SYRUP

Drowsiness, somnolence, fatigue, dry mouth, pharyngitis. Children: headache, pharyngitis, GI upset/pain, cough, somnolence, diarrhea, epistaxis, bronchospasm, fatigue, irritability, insomnia.

How is CHILDREN'S ZYRTEC HIVES RELIEF SYRUP supplied?

Tabs—5, 14, 30, 45, 75
Liquid gels—12, 25, 40
Chew tabs 5mg—5
10mg—12, 24
Prefilled spoons (5mL)—10
Hives Relief tabs—14
Syrups—4oz

Related Disease:

Allergic rhinitis~systemic products

Allergy~systemic antiallergic drugs

Urticaria~antihistamines

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June 25, 2010

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FDA warns against swallowing topical Benadryl gel

May 12, 2010

The FDA is warning consumers about potentially serious side effects from mistakenly swallowing McNeil Consumer & Specialty Pharmaceuticals' Benadryl (diphenhydramine) Extra Strength Itch Stopping Gel.

FDA launches "Bad Ad Program" to detect misleading drug ads

May 11, 2010

The FDA's Division of Drug Marketing, Advertising, and Communications (DDMAC) has launched the Bad Ad Program, designed to educate healthcare providers about their role in ensuring that prescription drug advertising and promotion is truthful, and not misleading.