Label: PREPARATION H MEDICATED WIPES- witch hazel cloth

  • NDC Code(s): 0573-0557-01, 0573-0557-02, 0573-0557-03, 0573-0557-04
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 2, 2024

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

  • Active ingredient

    Witch hazel 50%

  • Purpose

    Astringent

  • Uses

    • helps relieve the local itching and discomfort associated with hemorrhoids
    • temporary relief of irritation and burning

    aids in protecting irritated anorectal areas

  • 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.

  • Directions

    • open the lid on the top of the wipes pouch
    • peel back wipes seal, remove completely and discard
    • 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

  • Other information

    • for best results, flush only one or two wipes at a time

    store at 20-25°C (68-77°F)

  • Inactive ingredients

    aloe barbadensis leaf juice, anhydrous citric acid, cocamidopropyl betaine, cocamidopropyl dimethylamine, diazolidinyl urea, dichloroacetic, dimethylaminopropylamine, glycerin, methylparaben, monochloroacetic acid, potassium sorbate, propylene glycol, sodium benzoate, sodium chloride, sodium citrate, sodium glycolate, water

  • Questions or comments?

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

  • Additional information

    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.

    Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

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

    Trademarks owned or licensed by GSK

    ©2022 GSK or licensor

  • Principal Display Panel

    PREPARATIONH

    Medicated Wipes

    HEMORRHOIDAL WIPES

    WITH WITCH HAZEL

    gentle, everyday cleansing to reduce irritation

    FLUSHABLE & SEPTIC SAFE

    • Cools, Soothes and Comforts
    • Convenient, Easy to Use
    • For Hemorrhoidal and Vaginal Care

    WITH ALOE

    3 60 COUNT POUCHES

    180 MEDICATED WIPES

    6 x 5 in. (15.2 x 12.7 cm)

    000077729 Front Carton

    PreparationH Medicated Wipes 180 ct
  • INGREDIENTS AND APPEARANCE
    PREPARATION H MEDICATED WIPES 
    witch hazel cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0573-0557
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL5 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCAMIDOPROPYL DIMETHYLAMINE (UNII: L36BM7DG2T)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    DICHLOROACETIC ACID (UNII: 9LSH52S3LQ)  
    3-DIMETHYLAMINOPROPYLAMINE (UNII: I98I2UEC03)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CHLOROACETIC ACID (UNII: 5GD84Y125G)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SODIUM GLYCOLATE (UNII: B75E535IMI)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0573-0557-0148 in 1 POUCH; Type 0: Not a Combination Product08/01/2022
    2NDC:0573-0557-022 in 1 CARTON08/01/2022
    248 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:0573-0557-033 in 1 CARTON08/01/2022
    360 in 1 POUCH; Type 0: Not a Combination Product
    4NDC:0573-0557-044 in 1 CARTON08/01/2022
    448 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01508/01/2022
    Labeler - Haleon US Holdings LLC (079944263)