- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
Do not use
- if you have kidney disease
- if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing cetirizine
When using this product
- drowsiness may occur
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careful when driving a motor vehicle or operating machinery
Stop use and ask doctor if
- you have trouble urinating or emptying your bladder
- an allergic reaction to this product occurs. Seek medical help right away.
-
Directions
adults 65 years of age and older - ask a doctor
adults and children 12-64 years of age - take 1 tablet (5 mg) once daily in the evening
- do not take more than 1 tablet (5 mg) in 24 hours
- 1/2 tablet (2.5 mg) once daily in the evening may be appropriate for less severe symptoms
children 6-11 years of age - take 1/2 tablet (2.5 mg) once daily in the evening
- do not take more than 1/2 tablet (2.5 mg) in 24 hours
children under 6 years of age - do not use
consumers with kidney disease - do not use
- Other information
- Inactive ingredients
- Questions or comments?
-
Carton Label
LEADER
NDC 70000-0362-2
Original Prescription Strength
24HR Allergy Relief
Levocetirizine Dihydrochloride
Tablets USP, 5 mg I Antihistamine24 Hour Relief of
Sneezing, Runny Nose
Itchy Nose or Throat, and
Itchy, Watery EyesCOMPARE TO XYZAL®
ALLERGY 24HR
active ingredient*100% Money
Back Guarantee35 TABLETS
- Bottle Label
-
INGREDIENTS AND APPEARANCE
24HR ALLERGY RELIEF
levocetirizine dihydrochloride tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0362(NDC:43598-735) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength levocetirizine dihydrochloride (UNII: SOD6A38AGA) (levocetirizine - UNII:6U5EA9RT2O) levocetirizine dihydrochloride 5 mg Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM STEARATE (UNII: 70097M6I30) HYPROMELLOSES (UNII: 3NXW29V3WO) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A) Product Characteristics Color white Score 2 pieces Shape OVAL Size 9mm Flavor Imprint Code L Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-0362-2 1 in 1 CARTON 03/12/2018 1 35 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:70000-0362-1 2 in 1 CARTON 08/14/2018 2 5 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA210375 03/12/2018 Labeler - CARDINAL HEALTH (063997360)