Label: ALLEXPERT 24HR ANTIHISTAMINE CETIRIZINE HYDROCHLORIDE ORAL SOLUTION- allexpert 24hr antihistamine cetirizine hydrochloride solution

  • NDC Code(s): 84264-001-01
  • Packager: Bowong Technology (ShenZhen) Co.,Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated April 17, 2024

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  • Active Ingredient(s)

    Cetirizine HCI 5mg.(in each 5ml)

  • Purpose

    Antihistamine

  • Use

    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    ■Runny nose
    ■Sneezing
    ■Itchy, watery eyes
    ■Itching of the nose or throat

  • Warnings

    1.ASK A DOCTOR before use if you have Iver or kidney disoaso. Your doctor should dotermine iI you need a dilferent dose.
    2.ASK A DOCTOR or phamaclst belore use i you aro taking tranqulzors or sodativcs.

  • Do not use

    if you have over had an allorgic reaclion lo ths product or any ol ils ingredients or to an anlihislamine conlaining hydroxydine
    or other Piperazine derivatives .

  • WHEN USING

    ■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

    if an allergic reoclion lo this product occurs. Seek medical help right away.

  • KEEP OUT OF REACH OF CHILDREN

    In cose of overdose. get medical help or contact a Poison Control Center right away.

  • Directions

    See Outer box

  • Other information

    ■store between 20* to 25C (68* to 77*F)

    ■see bottom panel for lot number and expiration date.

  • Inactive ingredients

    Sodium Dihydrogen Phosphate, Dibasic
    Sodium Phosphate, Sodium Benzoate,
    Aspartame, purified water.

  • Package Label - Principal Display Panel

    labellabel1

  • INGREDIENTS AND APPEARANCE
    ALLEXPERT 24HR ANTIHISTAMINE CETIRIZINE HYDROCHLORIDE ORAL SOLUTION 
    allexpert 24hr antihistamine cetirizine hydrochloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84264-001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ASPARTAME (UNII: Z0H242BBR1)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    WATER (UNII: 059QF0KO0R)  
    AZITHROMYCIN SODIUM DIHYDROGEN PHOSPHATE (UNII: ADV7FS82PV)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84264-001-01150 mL in 1 BOTTLE; Type 0: Not a Combination Product04/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/17/2024
    Labeler - Bowong Technology (ShenZhen) Co.,Ltd (844456666)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bowong Technology (ShenZhen) Co.,Ltd844456666manufacture(84264-001)
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