Label: CHILDRENS ALLERGY RELIEF- diphenhydramine hcl solution

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

Drug Label Information

Updated January 22, 2025

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

  • ACTIVE INGREDIENT

    Drug Facts

    Active ingredients

    (in each 5 mL teaspoonful)

    Diphenhydramine HCl 12.5 mg

  • PURPOSE

    Purpose

    Antihistamine

  • INDICATIONS & USAGE

    Uses

    temporarily relieves these symptoms due to hay fever or other respiratory allergies:
          ■ sneezing
          ■ itching of the nose or throat
          ■ runny nose
          ■ itchy watery eyes
    ■temporarily relieves these symptoms due to the common cold:
          ■ sneezing
          ■ runny nose

  • WARNINGS

    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
    ■ glaucoma
    ■ a breathing problem such as chronic bronchitis

  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if the child is taking sedatives or tranquillizers

  • WHEN USING

    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

    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)

  • DOSAGE & ADMINISTRATION

    Directions
    ■ if needed, take every 4-6 hours
    ■ do not take more than 6 doses in 24-hours

     children under 4 years of age Do not use
     children 4 to under 6 years of age Do not use unless directed by a
     doctor
     children 6 to under 12 years of age 1 to 2 teaspoonfuls
    (5 ml to 10 ml)

  • OTHER SAFETY INFORMATION

    Other information
    Keep carton for full directions for use
    Each teaspoonful contains: sodium 10 mg
    ■ store at 20 - 25º C (68 - 77" F)
    ■ dosage cup provided

  • INACTIVE INGREDIENT

    Inactive ingredients

    citric acid, D&C red # 33, FD&C Red #40, flavor, glycerin, poloxamer 407, purified water, sodium benzoate, sodium
    chloride, sodium citrate, sucrose

  • QUESTIONS

    Questions? Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944

  • -----------

    Product Label: Best Choice® Children's Allergy Relief

    Best Choice®

    Children's Allergy Relief

    Diphenhydramine HCl

    Oral Solution

    Antihistamine

    Cherry Flavor

    8 FL OZ (237 mL)

    * This product is not manufactured or distributed by McNeil PPC, Inc., distributor of Benadryl® Allergy Liquid.

    PROUDLY DISTRIBUTED BY: VALU MERCHANDISERS, CO.
    5000 KANSAS AVE, KANSAS CITY, KS 66106

    Carton

    505-26 Crtn

    Bottle

    505-26 Botl

    res

  • INGREDIENTS AND APPEARANCE
    CHILDRENS ALLERGY RELIEF 
    diphenhydramine hcl solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63941-505
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HCL (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HCL12.5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID (UNII: 2968PHW8QP)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63941-505-261 in 1 CARTON01/01/2025
    1237 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01201/01/2025
    Labeler - Best Choice (868703513)
    Registrant - AptaPharma Inc. (790523323)
    Establishment
    NameAddressID/FEIBusiness Operations
    AptaPharma Inc.790523323manufacture(63941-505)