Label: WITCH HAZEL liquid

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

Drug Label Information

Updated December 11, 2024

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  • ACTIVE INGREDIENT

    Witch Hazel 100% (Containing alcohol 14% by Volume)

  • PURPOSE

    Astringent

  • INDICATIONS & USAGE

    Use for relief of minor skin irritations due to

    • Insect bites
    • minor cuts
    • minor scrapes
  • WARNINGS

    For External use only

    Avoid contact with eyes. If contact occurs, rinse thoroughly with water

    Stop use and ask a doctor if

    • condition worsens or symptoms last for more than 7 days

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

  • DOSAGE & ADMINISTRATION

    Apply as often as needed

  • INACTIVE INGREDIENT

    Alcohol

  • PRINCIPAL DISPLAY PANEL

    Bottle front labelBottle back label

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-330
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL84 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-330-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product02/24/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/24/2023
    Labeler - CVS HEALTH (062312574)
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