Label: HAZEL PERINEAL HEALING FOAM- witch hazel liquid

  • NDC Code(s): 84506-001-01, 84506-001-02
  • Packager: SHANGHAI SENWO INDUSTRY CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 4, 2024

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  • ACTIVE INGREDIENT

    Witch Hazel 50%

  • PURPOSE

    Astringent

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children lfswallowed,get medica help or contact aPoison Control Center right away.

  • INDICATIONS & USAGE

    Helps relieve pain and swelling from hemorrhoids and childbirth.

  • WARNINGS

    For external use only

  • DOSAGE & ADMINISTRATION

    When using this product m Avoid contact with eyes.lf contact occurs.rinsethoroughly with water..Do not exceed the recommended daily dosage unlessdirected by a doctor m Do not put this product into the rectum by using fingeror any mechanical device or applicator.

  • STORAGE AND HANDLING

    Other informationm Store at room temperature Single use per wipe

  • INACTIVE INGREDIENT

    Water
    C12-18 ALKYL GLUCOSIDE
    SODIUM LAUROYL SARCOSINATE
    SODIUM LAUROYL GLUTAMATE
    COCAMIDOPROPYL BETAINE
    ERYTHRITOL
    BUTYLENE GLYCOL
    ALCOHOL
    HYDROXYACETOPHENONE
    1,2-HEXANEDIOL
    PHENOXYETHANOL
    TOCOPHEROL
    SAURURUS CHINENSIS LEAF/ROOT
    EXTRACT
    TARAXACUM OFFICINALE
    (DANDELION) LEAF EXTRACT
    STEPHANIA TETRANDRA EXTRACT
    MENTHA HAPLOCALYX OIL
    CITRIC ACID
    PEG-40 HYDROGENATED CASTOR OIL

  • PRINCIPAL DISPLAY PANEL

    labellabel2

  • INGREDIENTS AND APPEARANCE
    HAZEL PERINEAL HEALING FOAM 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84506-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL50 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    TARAXACUM OFFICINALE (UNII: 39981FM375)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)  
    ERYTHRITOL (UNII: RA96B954X6)  
    ALCOHOL (UNII: 3K9958V90M)  
    STEPHANIA TETRANDRA WHOLE (UNII: 7S7TV2F4XC)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    SAURURUS CHINENSIS WHOLE (UNII: 6DRV3D37XS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84506-001-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product07/04/2024
    2NDC:84506-001-02150 mL in 1 BOTTLE; Type 0: Not a Combination Product07/04/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01507/04/2024
    Labeler - SHANGHAI SENWO INDUSTRY CO., LTD. (421273994)
    Establishment
    NameAddressID/FEIBusiness Operations
    SHANGHAI SENWO INDUSTRY CO., LTD.421273994manufacture(84506-001)
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