Label: DIPHENHYDRAMINE ORAL LIQUID- diphenhydramine hydrochloride liquid

  • NDC Code(s): 57237-305-12, 57237-305-16
  • Packager: Rising Health, LLC
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 13, 2022

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient in each 5 mL ( in one teaspoonful)

    Diphenhydramine HCl, 12.5 mg

  • Purpose

    Antihistamine

  • Uses

    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

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

    temporarily relieves these symptoms due to the common cold:

    • runny nose
    • sneezing
  • Warnings

    Do not use

    • with any other product containing diphenhydramine, even one used on skin.

    Ask a doctor before use if you have

    • glaucoma
    • trouble urinating due to an enlarged prostate gland
    • a breathing problem such as emphysema or chronic bronchitis.
    • a sodium-restricted diet

    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.

    Directions

    • take every 4-6 hours
    • Do not use more than 6 dose in 24 hours
    adults and children 12 years of age and over2 to 4 teaspoonfuls (25 to 50 mg)
    children 6 to under 12 years of age1 to 2 teaspoonfuls (12.5 to 25 mg)
    children under 6 yearsask a doctor

  • Other information

    • store at room temperature 15º - 30ºC (59º - 86ºF)
    • protect from freezing
    • protect from light
    • each teaspoon (5 mL) contains: sodium 8 mg

    TAMPER EVIDENT: DO NOT USE THIS PRODUCT IF BREAKAWAY BAND ON CAP IS BROKEN OR MISSING.

  • Inactive ingredients

    cherry flavor, citric acid, D & C Red #33, FD & C Red #40, flavor, sodium benzoate, sodium citrate, sodium saccharin, sorbitol, sucrose, water.

    Questions or comments?

    1-844-474-7464

  • PRINCIPAL DISPLAY PANEL

    Rising Health, LLC

    NDC 57237-305-12

    Diphenhydramine Hcl 12.5 mg/5 mL Oral Solution

    4 fl oz (118 mL)

    diphenhydramine-label

  • INGREDIENTS AND APPEARANCE
    DIPHENHYDRAMINE ORAL LIQUID 
    diphenhydramine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57237-305
    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)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Sodium Citrate (UNII: 1Q73Q2JULR)  
    Saccharin Sodium (UNII: SB8ZUX40TY)  
    Sorbitol (UNII: 506T60A25R)  
    Sucrose (UNII: C151H8M554)  
    Water (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorPINK (dark pink to pink) Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57237-305-12118 mL in 1 BOTTLE; Type 0: Not a Combination Product12/19/2022
    2NDC:57237-305-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product12/19/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34112/19/2022
    Labeler - Rising Health, LLC (080500961)
    Establishment
    NameAddressID/FEIBusiness Operations
    Invahealth Inc.116840615manufacture(57237-305) , pack(57237-305) , label(57237-305) , analysis(57237-305)
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