CETIRIZINE HYDROCHLORIDE description, usages, side effects, indications, overdosage, supplying and lots more!

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CETIRIZINE HYDROCHLORIDE

Apotheca Inc.

Cetirizine 10mg Tablets, Allergy Tablets DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT



PURPOSE



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

WARNINGS

Do Not Use

Ask a Doctor before use

Ask a Doctor or Pharmacist before use

if you are taking tranquilizers or sedatives.

When using this product

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

Stop use and ask a doctor

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 Poison Control Center right away.

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.
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

Other information and inactive ingredients

  • store between 20° to 25°C (68° to 77°F)

anhydrous lactose, colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, sodium lauryl sulfate, titanium dioxide, and triacetin

Questions

Call 1-800-262-5244

Monday though Friday 9AM – 2PM MST

Distributed by:

RejuviLife, Phoenix, AZ

RejuviLife is a trademark of Apotheca Inc.

PACKAGE LABEL AND PRINCIPAL DISPLAY PANEL



Antihistamine
Indoor and Outdoor Allergies







CETIRIZINE HYDROCHLORIDE

CETIRIZINE HYDROCHLORIDE

CETIRIZINE HYDROCHLORIDE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:12634-987(NDC:0378-3637)
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
cellulose, microcrystalline
MAGNESIUM STEARATE
hypromellose
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
white (WHITE) 8 mm M;C37 BULLET

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:12634-987-96 6 in 1 BOTTLE, PLASTIC
2 NDC:12634-987-97 7 in 1 BOTTLE, PLASTIC
3 NDC:12634-987-00 10 in 1 BOTTLE, PLASTIC
4 NDC:12634-987-80 20 in 1 BOTTLE, PLASTIC
5 NDC:12634-987-71 30 in 1 BOTTLE, PLASTIC
6 NDC:12634-987-50 50 in 1 BOTTLE, PLASTIC
7 NDC:12634-987-01 100 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076677 2010-01-01


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