Label: CHILDRENS ALLERGY RELIEF DYE-FREE- diphenhydramine hcl solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 19, 2023

If you are a consumer or patient please visit this version.

  • Active ingredient (in each 5 mL)

    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 a doctor before use if the child has

    • a breathing problem such as chronic bronchitis
    • glaucoma

    Ask a doctor or pharmacist before use if the child is

    taking sedatives or tranquilizers.

    When using this product

    • marked drowsiness may occur
    • sedatives and tranquilizers may increase drowsiness
    • excitability may occur, especially in children

    Keep out of reach of children.

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

  • Directions

    • do not take more than directed
    • find right dose on chart below
    • mL = milliliter
    • only use the dose cup provided
    • take every 4 to 6 hours, or as directed by a doctor
    • do not take more than 6 doses in 24 hours
     Age (yr)Dose (mL)
    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 5 mL to 10 mL
  • Other information

    • each 5 mL contains: sodium 4 mg
    • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
    • see end flap for expiration date and lot number
  • Inactive ingredients

    anhydrous citric acid, flavor, glycerin, propylene glycol, purified water, sodium benzoate, sodium chloride, sodium citrate dihydrate, sucralose, xanthan gum

  • Questions or comments?

    Call 1-800-910-6874

  • Principal Display Panel

    NDC 11673-918-36

    Compare to active
    ingredient in
    Children's Benadryl®
    Dye-Free Allergy
    *

    dye-free

    children's
    allergy
    relief

    diphenhydramine HCl 12.5 mg
    per 5 mL oral solution/antihistamine

    alcohol and sugar free

    for relief of:

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

    up & up

    BUBBLEGUM
    FLAVOR
    AGES
    6-11
    YEARS

    4 FL OZ (118 mL)

    *This product is not manufactured or distributed by
    Kenvue Inc., owner of the registered trademark
    Children’s Benadryl® Dye-Free Allergy.
    50844 REV0123A01836

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED
    SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

    100% satisfaction guaranteed
    or your money back.

    Each year we give 5% of our profit to
    communities. See all the good we do 
    together at Target.com/Community.

    Distributed by Target Corporation
    Minneapolis, MN 55403
    TM & ©2023 Target Brands, Inc.

    Target 44-018

    Target 44-018

  • INGREDIENTS AND APPEARANCE
    CHILDRENS ALLERGY RELIEF  DYE-FREE
    diphenhydramine hcl solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-918
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorBUBBLE GUMImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-918-361 in 1 CARTON05/20/2018
    1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/20/2018
    Labeler - Target Corporation (006961700)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305manufacture(11673-918) , pack(11673-918)