Home – CETIRIZINE HYDROCHLORIDE
CETIRIZINE HYDROCHLORIDE
REMEDYREPACK INC.
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
OTC - ACTIVE INGREDIENT
OTC - PURPOSE
USES
WARNINGS
OTC - ASK DOCTOR
OTC - ASK DOCTOR/PHARMACIST
OTC - WHEN USING
OTC - STOP USE
OTC - PREGNANCY OR BREAST FEEDING
OTC - KEEP OUT OF REACH OF CHILDREN
DIRECTIONS
| adults and children 6 years and over |
1 to 2 tablets once daily; depending upon severity of symptoms; do not take
more than 2 tablets in 24 hours |
| adults 65 years and over |
1 tablet once a day; do not take more than 1 tablet in 24 hours |
| children under 6 years of age |
ask a doctor |
| consumers with liver or kidney disease |
ask a doctor |
STORAGE AND HANDLING
INACTIVE INGREDIENT
HOW SUPPLIED
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION
CETIRIZINE HYDROCHLORIDE
CETIRIZINE HYDROCHLORIDE TABLET
Product Information
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|
Product Type
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Human prescription drug label |
Item Code (Source)
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NDC:49349-105(NDC:60505-2633) |
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Route of Administration
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ORAL |
DEA Schedule
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Product Characteristics
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Color
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Size
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Imprint Code
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Shape
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white |
6 mm |
APO;10;MG |
SQUARE |
Packaging
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#
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Item Code
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Package Description
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Marketing Start Date
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Marketing End Date
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1 |
NDC:49349-105-02 |
30 in 1 BLISTER PACK |
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Marketing Information
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Marketing Category
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Application Number or Monograph Citation
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Marketing Start Date
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Marketing End Date
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|
ANDA |
ANDA078317 |
2010-12-01 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
