Label: WITCH HAZEL- witch hazel spray spray

  • NDC Code(s): 41250-383-06
  • Packager: Meijer Distribution Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 9, 2024

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  • Active ingredient

    Witch Hazel 86%

  • Purpose

    Astringent

  • Uses

    Relieves minor skin irritation due to:

    • insect bites
    • minor cuts
    • minor scrapes
  • Warnings

    For external use only.

    Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F. Keep out of the reach of children. Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

    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
    • 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 necessary
    • to apply to face, moisten cotton ball or cleansing pad and gently wipe skin
  • Other information

    store at room temperature

  • Inactive ingredient

    alcohol (14%)

  • Questions?

    Call 1-866-964-0939

  • Principal Display Panel

    meijer

    CONTINUOUS

    witch

    hazel

    Astringent Spray

    For Face and Body

    Soothes irritated,

    inflamed, oily, or

    blemished skin

    NET WT 6.0 0Z (170 g)

    witch hazel

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-383
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL146 g  in 170 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-383-06170 g in 1 CAN; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/01/2021
    Labeler - Meijer Distribution Inc (006959555)
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