Label: WITCH HAZEL liquid

  • NDC Code(s): 70000-0615-1
  • Packager: Cardinal Health (Leader) 70000
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 4, 2025

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  • Active ingredient

    Witch hazel, USP 86%

  • Purpose

    Astringent

  • Uses

    • for relief of minor skin irritations due to:
      • insect bites
      • minor cuts
      • minor scrapes
  • Warnings

    For external use only.

    • Avoid swallowing.

    When using this product

    avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor if

    condition worsens or symptoms persist for more than 7 days

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away..

  • Directions

    apply to the affected area as often as necessary.

  • Other information

    • keep tightly closed
    • store at room temperature
  • Inactive ingredient

    alcohol 14% by volume

  • Questions or comments?

    Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

  • Principal Display Panel

    COMPARE TOT.N. DICKINSON'S® WITCH HAZEL active ingredient*

    Witch Hazel

    USP, 86% | Astringent

    Alcohol 14% by Volume

    Hamamelis Water

    For relief of

    Minor Skin Irritations

    Due To:

    Insect Bites

    Minor Cuts

    Minor Scrapes

    FL OZ (mL)

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

    TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

    DIST. BY

    CAH DUBLIN, OH 43017

    www.myleader.com

  • Package Label

    Witch Hazel, USP 86%

    LEADER Witch Hazel

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0615
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL842 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70000-0615-1473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/30/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/30/2022
    Labeler - Cardinal Health (Leader) 70000 (063997360)
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