Label: MEDIQUE CETIRAMED- cetirizine hcl tablet, coated

  • NDC Code(s): 47682-204-46, 47682-204-50
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 19, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Drug Facts

  • Active ingredient

    Cetirizine HCl 10 mg

  • Purpose

    Antihistamine

  • Uses

    T emporarily relieves these symptoms due to hay fever or other upper respiratory allergies

    • runny nose
    • itchy, watery eyes
    • sneezing
    • itching of the nose or throat
  • Warnings

    Do not use

    if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing 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 pharmacists before use if you are taking tranquilizers or sedatives.

    When using this product

    • drowsiness may occur
    • avoid alcoholic beverages
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery
  • STOP USE

    Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding

    • if breast feeding: not recommended
    • if pregnant: ask a health professional before use
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center
    (1-800-222-1222) right away.

  • Directions

    Adults and children: (6 years and older) one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours.

    Adults over 65 years: Ask a doctor

    Children under 6 years: Ask a doctor

    Consumers with liver or kidney disease: Ask a doctor

  • OTHER SAFETY INFORMATION

    Other information

    • store between 68º and 77ºF (20º and 25ºC)
    • tamper evident sealed packets
    • do not use any opened or torn packets
    • contains no ingredient made from a gluten-containing grain (wheat, barley or rye)
  • INACTIVE INGREDIENT

    colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

  • Questions or comments?

    Call 1-800-634-7680

  • Medique Cetiramed Label

    Medique®

    Collect MediBucks

    See inside flap for more details

    Cetiramed

    24-Hour Allergy Relief

    24-horas alivio a las alergias

    Pull To Open

    Tire Para Abrir

    Allergy Relief • Cetirizine HCl 10 mg

    Alivio a las aletgias • Cetirizina HCl 10 mg

    50 Tablets (50 x 1)

    Tamper Evident Unit Dose Packets

    Empaquetado con Sellado Evidente en Dosis Unitarias

    MDQ

  • INGREDIENTS AND APPEARANCE
    MEDIQUE CETIRAMED 
    cetirizine hcl tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-204
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite ((white to off white)) Score2 pieces
    ShapeRECTANGLE ((rounded off rectangle)) Size9mm
    FlavorImprint Code G;4
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-204-5050 in 1 BOX04/06/202011/30/2024
    11 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-204-461 in 1 PACKET; Type 0: Not a Combination Product04/06/202011/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20927404/06/202011/30/2024
    Labeler - Unifirst First Aid Corporation (832947092)