Label: ALL DAY ALLERGY ANTIHISTAMINE- cetirizine hcl tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 59726-220-14 - Packager: P and L Development of New York Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 20, 2012
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- Official Label (Printer Friendly)
- Active Ingredient (in each tablet)
- Purpose
- Uses
- WarningsDo not use
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if you are
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children
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Directions
Adults and children 6 years and over Take 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 - Other Information
- Inactive Ingredients
- Questions or comments?
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Principal Display Panel
†Compare to the active ingredient in Zyrtec®
24 Hour
All Day Allergy
Cetirizine HCl Tablets, 10 mg
Antihistamine
Allergy Relief of:
- Runny nose
- sneezing
- Itchy, watery eyes
- Itching of the nose or throat
Treats Indoor & Outdoor allergies
†This product is not manufactured or distributed by McNeil Consumer Healthcare Division of McNeil-PPC, Inc., owner of the registered trademark Zyrtec®
THIS PRODUCT IS PACKAGED IN A CHILD RESISTANT AND TAMPER EVIDENT PACKAGE. USE ONLY IF BLISTERS ARE INTACT.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
Distributed by:
PL Developments
Westbury, NY 11590
PRODUCT OF INDIA
- Product Label
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INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY ANTIHISTAMINE
cetirizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59726-220 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYPROMELLOSES (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A) POVIDONES (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color WHITE Score no score Shape OVAL Size 8mm Flavor Imprint Code W989 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59726-220-14 1 in 1 CARTON 1 14 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078427 12/05/2012 Labeler - P and L Development of New York Corporation (800014821) Registrant - P and L Development of New York Corporation (800014821)