Label: WITCH HAZEL- witch hazel spray spray

  • NDC Code(s): 56104-035-06
  • Packager: Premier Brands of America Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 13, 2024

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  • Active ingredient

    Witch Hazel

  • Purpose

    Astringent

  • Uses

    For relief of minor skin irritation due to

    • insect bites
    • minor cuts
    • minor scrapes
  • Warnings

    For external use only.

    Flammable:

    Avoid spraying in eyes. Content under pressure. Do not puncture or incinerate. Do not store at temperatures above 120 oF. Keep out of reach of children. Use only as directede. 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 rince thoroughly with water.

    Stop use and ask doctor of

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few 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
    • to apply to face, moisten cotton ball or cleansing pad and gently wipe skin
  • Other Information

    Store at room temperature

  • Inactive Ingredients

    Alcohol (14%)

  • Questions?

    1-866-964-0939

  • Principal Display Panel

    Premier

    Witch Hazel Continuous Spray

    Natural Astringent for face & body

    Cleanses & soothes skin that is:

    Irritated

    Inflamed

    Oily

    Blemished

    NET WT 6.0 OZ (170 g)

    PB_Witch Hazel.jpg

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-035
    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:56104-035-06170 g in 1 CAN; Type 0: Not a Combination Product03/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/01/2017
    Labeler - Premier Brands of America Inc (117557458)
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