SOOTHING HEMORRHOIDAL WIPES 50 WITCH HAZEL- witch hazel cloth

Soothing Hemorrhoidal Wipes 50 Witch Hazel by

Drug Labeling and Warnings

Soothing Hemorrhoidal Wipes 50 Witch Hazel by is a Otc medication manufactured, distributed, or labeled by The Honey Pot Company LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

SOOTHING HEMORRHOIDAL WIPES 50 WITCH HAZEL 
witch hazel cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82637-0059
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	500 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82637-0059-1	30 in 1 POUCH	09/01/2024
1		2.8 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	09/01/2024

Labeler - The Honey Pot Company LLC (045600502)