Label: SOOTHING HEMORRHOIDAL WIPES 50 WITCH HAZEL- witch hazel cloth

  • NDC Code(s): 82637-0059-1
  • Packager: The Honey Pot Company LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated August 1, 2024

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  • Drug Facts

  • Active Ingredient:

    Witch Hazel 50%

    Purpose:

    Astringent

  • Uses:

    • Helps relieve the local itching and discomfort associated with hemorrhoids
    • Temporary relief of irritation or 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 doctor if:

    • Bleeding occurs
    • If symptoms persist for more than 7 days, or clear up and reoccur again within a few days.

    Keep out of reach of of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Adults and children 12 years of age and older:

    • Unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area
    • Apply to the affected area up to 6 times daily or after each bowel movement

    Children under 12 years of age: Consult a doctor

  • Inactive Ingredients:

    water, alcohol, aloe barbadensis leaf juice, cucumis sativus (cucumber) fruit extract, chamomilla recutita (matricaria) flower extract, calendula officinalis flower extract, althaea officinalis root extract, avena sativa (oat) kernel extract, cocos nucifera (coconut) fruit extract, apple cider vinegar, honey, helianthus annuus (sunflower) seed oil, euterpe oleracea fruit extract, lactobacillus, lactobacillus ferment, punica granatum fruit extract, tocopheryl acetate, polyglyceryl-4 caprate, propylene glycol, cocamidopropyl PG-dimonium chloride phosphate, glycerin, disodium cocoamphodiacetate, sodium chloride, sodium glycolate, sodium hydroxide, tetrasodium glutamate diacetate, citric acid, phenoxyethanol, ethylhexylglycerin, fragrance

  • Other Information:

    Store at a controlled room temperature 77°F (20-25°C).

  • Questions:

    For questions and general information visit us at www.thehoneypot.co/contact

  • Prinicpal Display Panel:

    THE HONEY POT COMPANY

    PLANT-DERIVED INTIMATE CARE

    SOOTHING

    HEMORRHOIDAL

    wipes with witch hazel

    OBGYN – TESTED

    GENTLE + NON-IRRITATING

    TEMPORARY RELIEF OF IRRITATION + BURNING

    FLUSHABLE + SEPTIC SAFE

    HEMORRHOIDAL + VAGINAL CARE

    MAXIMUM STRENGTH

    20 WIPES

    7 x 5 in. (17.7 x 12.7 cm)

    Label

    Film

  • INGREDIENTS AND APPEARANCE
    SOOTHING HEMORRHOIDAL WIPES 50 WITCH HAZEL 
    witch hazel cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82637-0059
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL500 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    OAT (UNII: Z6J799EAJK)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    COCONUT (UNII: 3RT3536DHY)  
    CUCUMBER (UNII: YY7C30VXJT)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ACAI (UNII: 46AM2VJ0AW)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    HONEY (UNII: Y9H1V576FH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885)  
    POMEGRANATE (UNII: 56687D1Z4D)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    APPLE CIDER VINEGAR (UNII: 0UE22Q87VC)  
    ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BIFIDOBACTERIUM ANIMALIS LACTIS (UNII: 5307V7XW8I)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM GLYCOLATE (UNII: B75E535IMI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82637-0059-130 in 1 POUCH09/01/2024
    12.8 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01509/01/2024
    Labeler - The Honey Pot Company LLC (045600502)
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