Label: WITCH HAZEL liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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 September 13, 2022

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  • Active ingredient

    Witch hazel 86%

    Purpose

    Astringent

  • Use

     for relief of minor skin irritations due to:

    • insect bites 
    • minor cuts 
    • minor scrapes
  • Warnings

    For external use only

    When using this product

    • avoid contact with the eyes

    Stop use and ask a doctor if

    • condition worsens or symptoms persist for more than 7 days

    Keep out of reach of children.

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

  • Directions

    apply as often as needed

  • Inactive ingredient

     alcohol 14% by volume

  • SPL UNCLASSIFIED SECTION

    This product is not manufactured or distributed by Dickinson Brands, Inc., distributor of T.N. Dickinson's Witch Hazel.*

    Questions? call 1-800-910-6874

    245 07 0390 ID430463

    Distributed by Target corporation

    Minneapolis, MN 55403

    Made in USA

  • principal display panel

    NDC 11673-822-43

    witch hazel

    Compare to T.N. Dickinson's Witch Hazel*

    astringent

    facial cleanser

    helps soothe and relieve minor skin irritations

    UP + UP

    16 FL OZ (473.1 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL86 kg  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-822-43473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/29/1998
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/29/1998
    Labeler - Target Corporation (006961700)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(11673-822)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(11673-822)
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