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Dude Hemorrhoidal Wipes drug information

WITCH HAZEL
Dude Products · TOPICAL

Product NDC: 83731-055

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameWITCH HAZEL
Labeler / manufacturerDude Products
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC83731-055
Label effective date2026-08-25

Official product label reference

Dude Hemorrhoidal Wipes — Dude Products

This page contains 11 source sections for WITCH HAZEL, topical route. Label set fdf408ef-9392-a812-e053-6394a90a0017, version 5.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose

Purpose Astringent
Dosage and administration — label text
Dosage Can be used up to 6 times daily or after each bowel movement and before applying topical hemorrhoidal treatments.
Warnings
Warnings For external use only
Active ingredient
Active Ingredient Witch Hazel 25%
While using this medicine
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.
When to stop use and seek help
Stop use and ask a doctor if • Rectal bleeding occurs or; • If condition worsens or does not improve within 7 days
Child safety
Keep out of reach of children if swallowed, get medical help, or contact a Poison Control Center right away.
Storage and handling
Storage Storage: Store at room temperature.
Inactive ingredient
Inactive ingredients ALOE BARBADENSIS LEAF EXTRACT, DISODIUM COCOAMPHODIACETATE, GLUCONIC ACID, GLYCERIN, SODIUM BENZOATE, SODIUM CITRATE DIHYDRATE, TOCOPHERYL ACETATE, WATER
Questions
Questions or Comments 1-877-432-4411

Official sources and product identifiers

Substances listed: WITCH HAZEL

Package NDC codes

83731-055-48, 83731-055-03

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.