Label: WITCH HAZEL liquid

  • NDC Code(s): 63940-822-43
  • Packager: Liberty Procurement, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 September 27, 2023

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  • Active ingredients

    Witch Hazel 86%

  • Purpose

    Astringent

  • Use

    for relief of minor skin irritations due to:

    • insects bites
    • minor cuts
    • monor 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 worses or symptoms last 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 ingredients

    alcohol 14% by volume

  • SPL UNCLASSIFIED SECTION

    Distributed by

    Liberty Procurement, Inc

    650 Liberty Ave.

    Union, NJ 07083 USA

    Visit us at: www. facevalues.com

    SATIDFACTION GUARANTEED

    Or Your Money Back

  • principal display panel

    COREVLAUES

    Witch Hazel USP

    • Astringent - Cleans & refreshes face & body; Gentle, non-drying
    • Soothes & relieves minor skin irritations - Treats insect bites, minor cuts & scrapes

    16 FL OZ (1 PT) 473 mL

    image description

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL841 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63940-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/08/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34704/08/2011
    Labeler - Liberty Procurement, Inc (804085293)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(63940-822)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(63940-822)
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