Label: WITCH HAZEL- witch hazel liquid 

  • Label RSS
  • 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 04/13

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

  • Active ingredients

    Witch Hazel 86%

    Close
  • Purpose

    Astringent

    Close
  • Use

    for relief of minor skin irritations due to:

    • insect bites
    • minor cuts
    • minor scrapes
    Close
  • Warnings

    For external use only

    Close
  • When using this product

    avoid contact with the eyes

    Close
  • Stop use and ask a doctor if

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

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

    Close
  • Directions

    apply as often as needed

    Close
  • Inactive ingredient

    alcohol 14% by volume

    Close
  • Adverse Reactions

    DISTRIBUTED BY THE KROGER CO.

    CINCINNATI, OH 452O2

    For comments or questions please call 1-800=632-6900

    www.kroger.com

    Close
  • Principal Display Panel

    Kroger

    Quality Guaranteed

    WITCH

    HAZEL

    USP

    Hamamelis Water

    Astringent

    For relief of minot

    skin irritations due to:

    • Insect Bites
    • Minor Cuts
    • Minor Scrapes

    Alcohol 14% by volume

    16 FL OZ (1 PT) 473 mL

    image description

    Close
  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:30142-822
    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:30142-822-43 473 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part346 07/15/1989
    Labeler - kroger Co (006999528)
    Registrant - Vi-Jon (790752542)
    Establishment
    Name Address ID/FEI Business Operations
    Vi-Jon 790752542 manufacture(30142-822)
    Close