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 August 21, 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

    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

    For pump: Pump onto a clean pad and apply as often as needed.

  • Inactive ingredient

    alcohol 14% by volume

  • Questions?

    1-888-593-0593

  • SPL UNCLASSIFIED SECTION

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

    DIST. BY MEIJER DISTRIBUTION, INC

    GRAND RAPIDS, MI 49544

    www.meijer.com

  • principal display panel

    NDC 41250-822-43

    Compare to T.N. Dickson's Witch Hazel*

    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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