Label: WITCH HAZEL liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 28, 2023

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  • 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.

    • avoid swallowing

    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 persist for more than 7 days.

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    apply to the affected area as often as necessary.

  • Other information

    • keep tightly closed
    • store at room temperature
  • Inactive ingredient

    alcohol 14% by volume

  • Principal Display Panel

    Witch Hazel

    Alcohol 14% by Volume

    ASTRINGENT/HAMAMELIS WATER

    For Relief of minor skin irritations due to:

    • Insect bites
    • Minor cuts
    • Minor scrapes

    DISTRIBUTED BY: fred's, Inc.

    4300 NEW GETWELL RD

    MEMPHIS,TN 38118

    www.fredsinc.com

    Questions or comments:

    1-855-331-FRED (3733)

    FL OZ (mL)

    TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

  • Package Label

    Witch Hazel 86%

    FRED'S PHARMACY Witch Hazel

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55315-390
    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:55315-390-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/31/201406/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/31/201406/30/2024
    Labeler - Freds Inc (005866116)
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