Cetirizine Hydrochloride description, usages, side effects, indications, overdosage, supplying and lots more!

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Cetirizine Hydrochloride

McKesson
Orchid Chemicals & Pharmaceuticals Ltd.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Cetirizine HCl USP, 10 mg

Antihistamine

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

if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

liver or kidney disease. Your doctor should determine if you need a different dose.

taking tranquilizers or sedatives.

  • drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery.

and ask a doctor if an allergic reation to this product occurs. Seek medical help right away.

  • if breast-feeding: not recommended.
  • if pregnant: ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

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
  • TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.
  • store between 20° to 25°C (68° to 77°F).

corn starch, lactose monohydrate, povidone, magnesium stearate and opadry white.

The components of opadry white are: hydroxypropyl methylcellulose, polyethylene glycol 400, titanium dioxide.

call 1-866-562-4590

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton: 30 Tablets

Sunmark

COMPARE TO ZYRTEC®

ACTIVE INGREDIENT*

NDC 49348-939-44

24 hour

all day allergy

Cetirizine HCl Tablets USP, 10 mg

Antihistamine

6 Years and Older

Indoor & Outdoor Allergies

24 hour relief of: sneezing; runny nose;

itchy, watery eyes; itchy throat or nose

ORIGINAL PRESCRIPTION STRENGTH

30 TABLETS 10 mg EACH

Cetirizine Hydrochloride

Cetirizine Hydrochloride

Cetirizine Hydrochloride TABLET, FILM COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-939
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CETIRIZINE HYDROCHLORIDE CETIRIZINE 10 mg

Inactive Ingredients

Ingredient Name Strength
STARCH, CORN
lactose monohydrate
POVIDONE K29/32
MAGNESIUM STEARATE
Hypromellose 2910 (5 Mpa.s)
polyethylene glycol 400
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
white (white to off-white) 9 mm S;521 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE, PLASTIC
2 60 in 1 BOTTLE, PLASTIC
3 NDC:49348-939-12 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078862 2011-08-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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