Label: WITCH HAZEL liquid

  • NDC Code(s): 63941-822-43
  • Packager: Value Merchandisers, CO
  • 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 March 6, 2023

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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.  If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor if

    • condition worsens or symptoms persists 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

  • adverse reactons

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

    PROUDLTY DISTRIBUTED BY: VALUE MERCHANDISERS, CO. 5000 KANSAS AVE, KANSAS CITY, KS 66106

  • Principal Panel Display

    Best Choice

    Compare to T.N. Dickinson's Witch Hazel

    Witch

    Hazel

    U.S.P.

    • Astringent
    • For relief of minor skin irritations due to insect bites, minor cuts and scrapes
    • Cleanses, soothe, treat skin

    16 FL OZ (1 PT) 473 mL

    image description

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63941-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL860 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63941-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/21/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34712/21/2021
    Labeler - Value Merchandisers, CO (868703513)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(63941-822)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(63941-822)
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