Label: UNIVERSAL WITCH HAZEL- witch hazel solution

  • NDC Code(s): 52000-414-06
  • Packager: Universal Distribution Center LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • Drug Facts

  • Active Ingredients:

    All natural distilled witch hazel 100%
    (contains natural grain alcohol 14%)

  • Purpose

    Astringent

  • Usage:

    The soft toner is specifically developed to meet ultimate needs of purifying and conditioning for an array of skin types. It is a calm and non-drying formula which removes remaining traces of soap. It removes make-up or excess oils making your skin feeling soft, healthful, and smooth. It also smoothens the skin after shaving. Use as often as necessary. Apply directly from the bottle or dampen a cotton pad and smoothly wipe it off.

  • Warning:

    For external use only. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

    Keep out of reach of children.

  • Direction:

    • remove protective inner seal
    • moisten cotton ball or cleansing pad and gently wipe skin
    • apply as often as necessary

  • Ingredients:

    Water, Hamamelis Virginiana (Witch Hazel) Leaf Water, Alcohol (14% by Volume), Benzyl Alcohol, Methylchloroisothiazolinone, methylisothiazolinone.

  • SPL UNCLASSIFIED SECTION

    SKIN CLEANSER

    MAKE-UP REMOVER

    AFTER SHAVING

    For Face & Body

    Gentle Relief For

    100% NATURAL ASTRINGENT

    Specifically formulated for purifying and conditioning of the skin.

    Distributed by:
    Universal Distribution Center LLC
    Edison, NJ 08817
    www.universaldc.com

    This Product is Not Tested on Animals 

    Made in Jordan

  • Packaging

    WitchHazel-414

  • INGREDIENTS AND APPEARANCE
    UNIVERSAL WITCH HAZEL 
    witch hazel solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-414
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)  
    ALCOHOL (UNII: 3K9958V90M)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52000-414-06177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01607/01/2023
    Labeler - Universal Distribution Center LLC (019180459)
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