Label: CETIRIZINE HYDROCHLORIDE- cetirizine hydrochloride tablets tablet, film coated
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NDC Code(s):
71205-709-06,
71205-709-10,
71205-709-14,
71205-709-20, view more71205-709-30, 71205-709-60, 71205-709-90
- Packager: Proficient Rx LP
- This is a repackaged label.
- Source NDC Code(s): 43598-811
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 1, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistaminecontaining hydroxyzine.
Ask a doctor before use if you have
liver or kidney disease. Your doctor should determine if you need a different dose.
Ask a doctor or pharmacist before use if you are
Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.
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
Stop use and ask a doctor if
an allergic reaction to this product occurs. Seek medical help right away.
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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. 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?
- Bottle Label
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INGREDIENTS AND APPEARANCE
CETIRIZINE HYDROCHLORIDE
cetirizine hydrochloride tablets tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71205-709(NDC:43598-811) 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 HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STARCH, CORN (UNII: O8232NY3SJ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color WHITE Score no score Shape OVAL Size 7mm Flavor Imprint Code C Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71205-709-06 6 in 1 BOTTLE; Type 0: Not a Combination Product 10/31/2022 2 NDC:71205-709-10 10 in 1 BOTTLE; Type 0: Not a Combination Product 10/31/2022 3 NDC:71205-709-14 14 in 1 BOTTLE; Type 0: Not a Combination Product 10/31/2022 4 NDC:71205-709-20 20 in 1 BOTTLE; Type 0: Not a Combination Product 10/31/2022 5 NDC:71205-709-30 30 in 1 BOTTLE; Type 0: Not a Combination Product 10/31/2022 6 NDC:71205-709-60 60 in 1 BOTTLE; Type 0: Not a Combination Product 10/31/2022 7 NDC:71205-709-90 90 in 1 BOTTLE; Type 0: Not a Combination Product 10/31/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078343 12/17/2018 Labeler - Proficient Rx LP (079196022) Establishment Name Address ID/FEI Business Operations Proficient Rx LP 079196022 REPACK(71205-709) , RELABEL(71205-709)