DUDE HEMORRHOIDAL WIPES- witch hazel cloth

Dude Hemorrhoidal Wipes by

Drug Labeling and Warnings

Dude Hemorrhoidal Wipes by is a Otc medication manufactured, distributed, or labeled by Dude Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Witch Hazel 25%

Purpose

Astringent

Uses

Temporarily relieves these external symptoms associated with hemorrhoids:
Itching burning irritation

Warnings

For external use only

When using this product

Do not exceed the recommended daily dosage unless directed by a doctor.

Do not insert in rectum using fingers or mechanical device.

Stop use and ask a doctor if

Rectal bleeding occurs or;

If 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

As a hemorrhoidal treatment for adults:

When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly.

Gently dry by patting or blotting with toilet tissue or soft cloth before applying.
Gently apply to the affected area by patting and then discard.
Children under 12 years of age: Consult a doctor

Dosage

Can be used up to 6 times daily or after each bowel movement and before applying topical hemorrhoidal treatments.

Storage

Storage: Store at room temperature.

Inactive ingredients

ALOE BARBADENSIS LEAF EXTRACT, DISODIUM COCOAMPHODIACETATE, GLUCONIC ACID, GLYCERIN, SODIUM BENZOATE, SODIUM CITRATE DIHYDRATE, TOCOPHERYL ACETATE, WATER

Questions or Comments

1-877-432-4411

Package Label

INGREDIENTS AND APPEARANCE

DUDE HEMORRHOIDAL WIPES 
witch hazel cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83731-055
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	1.5 g

Inactive Ingredients
Ingredient Name	Strength
GLUCONIC ACID (UNII: R4R8J0Q44B)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83731-055-48	48 in 1 PACKAGE; Type 0: Not a Combination Product	01/14/2024
2	NDC: 83731-055-03	3 in 1 PACKAGE	12/31/2024
2	NDC: 83731-055-48	48 in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	01/14/2024

Labeler - Dude Products (078446360)