Label: UP AND UP CHILDRENS ALLERGY MELTS- diphenhydramine hcl tablet, chewable

  • NDC Code(s): 11673-012-18, 11673-012-48
  • Packager: Target Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2023

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  • Active ingredient (in each tablet)

    Diphenhydramine HCl 12.5 mg

  • Purpose

    Antihistamine

  • Uses

    ▪
     temporarily 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

    ▪
    to make a child sleepy
    ▪
    with any other product containing diphenhydramine, even one used on skin

    Ask your doctor before use if you have

    ▪
    a breathing problem such as emphysema or chronic bronchitis
    ▪
    glaucoma
    ▪
    trouble urinating due to an enlarged prostate gland

    Ask a doctor or pharmacist before use if you are

    taking sedatives or tranquilizers.

    When using this product

    ▪
    marked drowsiness may occur
    ▪
    avoid alcoholic drinks
    ▪
    alcohol, sedatives, and tranquilizers may increase drowsiness
    ▪
    be careful when driving a motor vehicle or operating machinery
    ▪
    excitability may occur, especially in children

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222

  • Directions

    ▪
    find right dose on chart below
    ▪
    Chew one tablet completely at the onset of symptoms. Do not swallow tablets whole.
    ▪
    take every 4 to 6 hours or as directed by a doctor
    ▪
    do not take more than 6 times in 24 hours

    children under 2 years

    do not use 

    children 2 to 5 years

    do not use unless directed by a doctor 

    children 6 to 11 years of age 

    1 to 2 chewable tablets (12.5 mg to 25 mg)

    adults and children 12 years of age and over

    2 to 4 tablets (25 mg to 50 mg)
  • Other information

    •
    store at room temperature. Avoid high humidity. Protect from light
  • Inactive ingredients

    citric acid, crospovidone, D&C Red No. 30, dextrose, FD&C Blue No. 1, flavors, magnesium stearate, maltodextrin, potassium citrate, silica, sodium polystyrene sulfonate, starch, sucralose.

  • Questions or comments?

     1-866-467-2748

  • Principal Display Panel

    Compare to active ingredient in Children's Benadryl® Allergy Chewables*

    Children’s Allergy relief
    Diphenhydramine HCl, 12.5 mg/ Antihistamine

    For relief of:

    •
    sneezing
    •
    runny nose
    •
    itchy throat
    •
    itchy, watery eyes

    4-6 Hours/Dose

    up & up

    Grape Flavor

    Naturally and Artificially Flavored

    TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

    *This product is not manufactured or distributed by Johnson & Johnson Consumer INC, owner of the registered trademark Children's Benadryl® Allergy Chewable Tablets*.


    Distributed by Target Corporation

    Minneapolis, MN 55403

    Made in USA
    TM & ©2020 Target Brands, Inc.

    100% satisfaction guaranteed or your money back.

    Children’s Allergy Grape Flavor 18 Chewable Tablets

    up and up childrens allergy melts 18 counts

    Children’s Allergy Grape Flavor 48 Chewable Tablets

    Childrens Allergy Relief 48 Chewable Tablets
  • INGREDIENTS AND APPEARANCE
    UP AND UP CHILDRENS ALLERGY MELTS 
    diphenhydramine hcl tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-012
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CROSPOVIDONE (120 .MU.M) (UNII: 68401960MK)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorPURPLEScore2 pieces
    ShapeROUNDSize16mm
    FlavorGRAPEImprint Code RP012
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-012-183 in 1 CARTON11/10/2015
    16 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:11673-012-484 in 1 CARTON10/30/2019
    212 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01211/01/2015
    Labeler - Target Corporation (006961700)
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