Label: CURIST ALLERGY RELIEF- levocetirizine dihydrochloride 5 mg tablet
- NDC Code(s): 72559-021-15
- Packager: Little Pharma, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 21, 2023
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
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 a doctor if
- you have trouble urinating or emptying your bladder
- an allergic reaction to this product occurs. Seek medical help right away.
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DOSAGE & ADMINISTRATION
Directions
adults 65 years and older ask a doctor adults and children 12-64 years - take 1 tablet (5 mg) once daily in the evening
- do not take more than 1 tablet (5 mg) in 24 hours
- ½ tablet (2.5 mg) once daily in the evening may be appropriate for less severe symptoms
children 6-11 years - take ½ tablet (2.5 mg) once daily in the evening
- do not take more than ½ tablet (2.5 mg) in 24 hours
children under 6 years do not use consumers with kidney disease do not use - STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CURIST ALLERGY RELIEF
levocetirizine dihydrochloride 5 mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72559-021 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 TITANIUM DIOXIDE (UNII: 15FIX9V2JP) HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POLYSORBATE 80 (UNII: 6OZP39ZG8H) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color white Score 2 pieces Shape OVAL Size 8mm Flavor Imprint Code LL;H Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72559-021-15 1 in 1 CARTON 01/24/2023 1 90 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA213513 01/24/2023 Labeler - Little Pharma, Inc. (074328189)