Label: WITCH HAZEL liquid

  • 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 July 1, 2021

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

  • Active ingredient

    Witch hazel 86%

  • Purpose

    Astringent

  • Uses

    For relief of minor skin irritations due to:

    • insect bites
    • minor cuts
    • minor scrapes
  • Warnings

    For external use only

  • When using this prodct

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

  • Stop use and ask a doctor if

    condition worsens or symptoms persis 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

  • adverse reaction

    DISTRIBUTED BY ONE EAST MAIN CO

    100 MISSION RIDGE

    GOODLETTSVILLE, TN 37072

    100%    Satisfaction Guaratneed

  • principal display panel

    DG| health

    Witch

    Hazel USP

    Astringent

    For relief of minor skin irritations due to:

    • Insect Bites
    • Minor Cuts
    • Minor Scraped

    100% Satisfaction Guaranteed! (888)309-9030

    16 FL OZ (1 PT) 473 mL

    image description

  • principal display panel

    Since 1903

    Rexall

    Witch

    Hazel

    Astringent

    For relief of minor skin irritations due to:

    • Insects bites
    • Minor cuts
    • Minor scrapes

    16 FL OZ (1PT) 473mL

    image description

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL979 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55910-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/05/1989
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34707/05/1989
    Labeler - OLD EAST MAIN CO. (068331990)
    Registrant - Vi Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC790752542manufacture(55910-822)