Label: WITCH HAZEL liquid

  • NDC Code(s): 68016-822-43
  • Packager: Pharmacy Vlaue Alliance LLC
  • 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 12, 2022

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

View All Sections
  • Active ingredient

    Witch hazel 86%

  • Purpose

    Astringent

  • use

    for relief of minor skin irritations due to:

    • insects 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

  • inactive ingredients

    alcohol 14% by volume

  • Questions

    Call 1-888-593-0593

  • SPL UNCLASSIFIED SECTION

    *This product is not manufactued or distributed by Dickinson Brand, Inc., distributorof T.N. Dickinson Witch Hazel.

    If for any reason you are not satisfied with this product, please return it to the store where purchased for a full refund.

    Distributed by: Phamacy Value Alliance LLC

    407 East Lancaster Avenue, Wayne, PA 19087

    www.emersongroup.com

  • Principal Panel Display

    COMPARE TO T.N.DICKINSON'S*

    Premier Value Witch Hazel u.s.p.

    astringent

    hamamelis water

    for relief of minor skin irritations due to:

    • insects bites
    • minor cuts
    • minor scrapes

    Square bottle uses less plastic than a similarly sized round bottle

    Recyclable ( if available in your area)

    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:68016-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL842 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68016-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2003
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34708/15/2003
    Labeler - Pharmacy Vlaue Alliance LLC (101668460)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(68016-822)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(68016-822)
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!