Label: WITCH HAZEL liquid

  • NDC Code(s): 11344-822-43
  • Packager: Consumer Product Partners, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 8, 2024

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

View All Sections
  • Active ingredients

    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 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 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

    Distributed by:

    V-Jon

    One Swan Drive

    Smyrna, TN 37167

  • Principal display panel

    swan ®

    WITCH HAZEL USP

    Hamamelis Water

    • Skin Astringent
    • For Relief of Minor Skin irritations Due to: Insect -Insect Bites - Minor Cuts -Minor Scrapes

    Square bottle uses less plastic than a similarly sized round bottle. Recycle (if available in your area)

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

    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:11344-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL860 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11344-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/29/1998
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01601/29/1998
    Labeler - Consumer Product Partners, LLC (119091520)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(11344-822)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(11344-822)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!