Label: CHILDRENS ALLERGY RELIEF- diphenhydramine hcl solution

  • NDC Code(s): 11822-0379-0, 11822-0379-1
  • Packager: Rite Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 22, 2024

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

    Do not use

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

    Ask a doctor before use if the child has

    •
    a breathing problem such as chronic bronchitis
    •
    glaucoma
    •
    a sodium-restricted diet

    Ask a doctor or pharmacist before use if the child is

    taking sedatives or tranquilizers

    When using this product

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

    Keep out of reach of children.

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

  • Directions

    •
    find right dose on chart below
    •
    mL = milliliter
    •
    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

    Attention: use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device.

  • Other information

    •
    each 5 mL contains: sodium 15 mg
    •
    store at 20-25°C (68-77°F). Protect from light. Store in outer carton until contents used.
    •
    do not use if printed neckband is broken or missing
  • Inactive ingredients

    anhydrous citric acid, D&C red #33, FD&C red #40, flavor, glycerin, high fructose corn syrup, poloxamer 407, purified water, sodium benzoate, sodium chloride, sodium citrate, sorbitol solution

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    Compare to the active ingredient in Children’s Benadryl® Allergy

    FREE FROM | GLUTEN FREE ALCOHOL FREE

    AGES 6-11

    CHILDREN’S ALLERGY RELIEF

    DIPHENHYDRAMINE HCl ORAL SOLUTION 12.5 mg / 5 mL ANTIHISTAMINE

    relieves:

    sneezing ● runny nose

    itchy, watery eyes

    itching of the nose or throat

    CHERRY FLAVOR

    DOSAGE CUP INCLUDED

    4 FL OZ (118 mL)

    Children's Allergy Relief Carton
  • INGREDIENTS AND APPEARANCE
    CHILDRENS ALLERGY RELIEF 
    diphenhydramine hcl solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0379
    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)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorRED (Bluish-Red) Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0379-01 in 1 CARTON04/05/2023
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:11822-0379-11 in 1 CARTON04/05/2023
    2237 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01204/05/2023
    Labeler - Rite Aid Corporation (014578892)
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