Label: WITCH HAZEL- 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

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 07/13

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

  • Active ingredients

    Witch Hazel 86%

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  • Purpose

    Astringent

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  • Use

    for relief of minor skin irritations due to:

    • insect bites
    • minor cuts
    • minor scrapes
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  • Warnings

    For external use only

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  • When using this product

    avoid contact with the eyes

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  • Stop use and ask a doctor if

    • condition worsens or symptoms persist for more than 7 days
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  • Keep out of reach of children

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

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  • Directions

    apply as often as needed

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  • Inactive ingredient 

    alcohol 14% by volume

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  • Adverse Reactions

    Manufactured by Vi-Jon, Inc.,

    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

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  • 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

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  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:37012-822
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WITCH HAZEL (WITCH HAZEL) WITCH HAZEL 979 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:37012-822-43 473 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part346 01/08/2008
    Labeler - Shopko Stores Operating Co., LLC (023252638)
    Registrant - Vi-Jon (790752542)
    Establishment
    Name Address ID/FEI Business Operations
    Vi-Jon 790752542 manufacture(37012-822)
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