Label: WITCH HAZEL liquid

  • NDC Code(s): 37012-822-43
  • Packager: Shopko Stores Operating Co., 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

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

  • 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

    Manufactured by Vi-Jon, LLC

    One Swan Drive., Smyrna, TN 37167

    ShopKo Stores Operating Co., LLC

    www.shopko.com

    for consumer questions call 1-888-593-0593

    ShopKo Satisfaction Guaranteed By Refund or Exchange

  • principal display panel

    ShopKo

    Witch Hazel U.S.P.

    Astringent

    For Relief of Minor Skin Irritations Due to:

    • Insects Bites
    • Minor Cuts
    • Minor Scrapes

    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:37012-822
    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:37012-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/08/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34601/08/2008
    Labeler - Shopko Stores Operating Co., LLC (023252638)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(37012-822)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(37012-822)