Label: WITCH HAZEL liquid

  • NDC Code(s): 41250-822-43, 41250-822-99
  • Packager: Meijer Distribution, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2024

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  • 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. If contact occurs, rinse thoroughly with water.

    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

  • Disclaimer

    *THIS PRODUCT IS NOT MANUFACTURED OR DISTRIBUTED BY DICKINSON BRANDS, INC., DISTRIBUTOR OF T.N. DICKINSON'S  WITCH HAZEL.

  • Adverse Reaction

    OUR QUALITY GUARANTEE

    The Meijer Family

    www.meijer.com/satisfaction

    DISTRIBUTED BY MEIJER DISTRIBUTION, INC.

    GRAND RAPIDS, MI 49544

    www.meijer.com

    PID 347719

    Pat. D675, 101

  • principal display panel

    NDC 41250-822-43

    COMPARE TO T.N. DICKINSON'S ® WITCH HAZEL ACTIVE INGREDIENTS*

    meijer

    Witch Hazel USP

    Astringent

    For Face & Body

    Cleans & Refreshes

    Soothes and relieves minor skin irritations

    16 FL OZ (473 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL86 kg  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-822-430.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/1996
    2NDC:41250-822-990.236 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/15/1996
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/15/1996
    Labeler - Meijer Distribution, Inc (006959555)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(41250-822)
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