Label: WITCH HAZEL liquid

  • NDC Code(s): 21130-822-43
  • Packager: Better Living Brands LLC
  • 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 12, 2022

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  • Active ingredients

    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 Dickson Brands, Inc., distributor of T.N. Dickinson's Witch Hazel

  • principal display panel

    NDC 21130-822-43

    Signature Care

    Quality Guaranteed

    Witch Hazel U.S.P.

    Astringent

    Relief of minor skin Irritations:

    • Insect bites
    • Minor cuts
    • Minor scrapes

    Compare to T.N. Dickinson's Witch Hazel active ingredient

    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:21130-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL979 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21130-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/18/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34606/18/2015
    Labeler - Better Living Brands LLC (009137209)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(21130-822)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(21130-822)
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