Label: PREPARATION H FOR WOMEN- witch hazel cloth

  • NDC Code(s): 0573-0559-10, 0573-0559-40, 0573-0559-41
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 1, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredient

    Witch hazel 20%

  • PURPOSE

    Purpose

    Astringent

  • INDICATIONS & USAGE

    Uses

    • helps relieve the local itching and discomfort associated with hemorrhoids
    • temporary relief of irritation and burning
    • aids in protecting irritated anorectal areas
  • WARNINGS

    Warnings

    For external use only

    When using this product

    • do not exceed the recommended daily dosage unless directed by a doctor
    • do not put this product into the rectum by using fingers or any mechanical device or applicator

    Stop use and ask a doctor if

    • bleeding occurs
    • condition worsens or does not improve within 7 days

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • open the lid on the top of the wipes pouch
    • grab the top wipe at the edge of the center fold and pull out of pouch
    • close lid after each use to retain moisture
    • adults: unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area.
    • use up to 6 times daily or after each bowel movement and before applying topical hemorrhoidal treatments, and then discard
    • children under 12 years of age: consult a doctor
  • STORAGE AND HANDLING

    Other information

    • store at 20-25°C (68-77°F)
    • for best results, flush only one or two wipes at a time
  • INACTIVE INGREDIENT

    Inactive ingredients

    aloe barbadensis leaf juice, anhydrous citric acid, capryl/capramidopropyl betaine, chamomilla recutita (matricaria) flower extract, cucumis sativus (cucumber) fruit extract, diazolidinyl urea, dipropylene glycol, DMDM hydantoin, edetate disodium, fragrance, glycerin, methylisothiazolinone, methylparaben, PEG-75 shea butter glycerides, phenoxyethanol, polysorbate 20, propylene glycol, propylparaben, purified water, sodium citrate, vitamin E acetate

  • QUESTIONS

    Questions or comments?

    Call weekdays 9 AM to 5 PM EST at 1-800-99PrepHor 1-800-997-7374

    For most recent product information,
    visit www.preparationh.com

  • Other Uses

    • for vaginal care– cleanse the area by gently wiping, patting or blotting. Repeat as needed.
    • for use as a moist compress– if necessary, first cleanse the area as previously described.

    Fold new wipe to desired size and place in contact with tissue for a soothing and cooling effect.

    Leave in place for up to 15 minutes and repeat as needed.

  • PRINCIPAL DISPLAY PANEL

    NDC 0573-0559-10

    PREPARATION H®
    MEDICATED HEMORRHOIDAL WIPES

    WITH WITCH HAZEL

    FOR Women
    FLUSHABLE & SEPTIC SAFE

    infused with refreshing
    CUCUMBER, SOOTHING ALOE,
    VITAMIN E, SHEA BUTTER & CHAMOMILE

    PreparationH ®Medicated Wipes are made with advanced technology, have been scientifically tested to be flushable and are safe for well-maintained sewer and septic systems*. They are made with 100% plant-based materials and are free from chemical binders. *Not recommended for use with basement pump systems. Flush only one wipe at a time.

    PAA113382 Front Carton

    PrepH Relief Wipes for Women 48 ct Front Carton
  • INGREDIENTS AND APPEARANCE
    PREPARATION H FOR WOMEN 
    witch hazel cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0573-0559
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL2 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CAPRYL/CAPRAMIDOPROPYL BETAINE (UNII: 231H3ZT9NE)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CUCUMBER (UNII: YY7C30VXJT)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0573-0559-1010 in 1 CARTON04/01/2014
    11 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:0573-0559-401 in 1 CARTON04/01/2014
    248 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:0573-0559-4148 in 1 POUCH; Type 0: Not a Combination Product04/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01504/01/2014
    Labeler - Haleon US Holdings LLC (079944263)