Label: XPECT EXTRA STRENGTH ITCH RELIEF- diphenhydramine hydrochloride spray

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

Drug Label Information

Updated December 28, 2023

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

  • Active ingredients

    Diphenhydramine hydrochloride 2%

  • Purpose

       External Analgesic

  • Uses

    for temporary relief of pain and itching associated with minor skin irritations and rashes due to insect bites, poison oak and poison sumac

  • Warnings

    For external use only

  • Do not use

    • on large areas of the body
    • with any other product containing diphenhydramine hydrochloride, even one taken by mouth
  • Ask a doctor before use

    • on chicken pox
    • on measles
  • When using this produt

    • avoid contact with the eyes
  • Stop use and ask a doctor if

    • condition worsens symptoms persist more than 7 days or clear up and occur again within a few days
  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • do not use more than directed
    • adults & children 12 years and over: apply to affected area not more than 3 to 4 times daily
    • children under 12: consult a doctor
  • ​Other information

    • store at room temperature
  • Inactive Ingredients

    germaben II, edetate disodium, glycerin, tomadol 25-9, purified water, triethanolamine

  • Questions?

    1-877-973-2811 M-F 8am-5pm

  • Package Principal Display Panel

    Extra Strength

    ITCH RELIEF

    Quick Itch & Pain Relief

    Diphenhydramine HCl 2%

    Convenient pump spray allows no-touch application. Use as a first aid treatment for insect bites and rashes from poison ivy, oak & sumac. 

    2 fl. oz. (59.1 mL)

    Xpect® First aid

    Bottle

  • INGREDIENTS AND APPEARANCE
    XPECT EXTRA STRENGTH ITCH RELIEF 
    diphenhydramine hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42961-218
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    C12-15 PARETH-9 (UNII: H3ZIY6WP1R)  
    water (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42961-218-0159.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/16/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/16/2022
    Labeler - Cintas Corporation (056481716)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America, Inc874965262manufacture(42961-218)