DUDE Hemorrhoidal Wipes

Manufacturer
Dude Products
Effective date
2026-08-25
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-08-27 00:01:35

Label at a glance#

ProductDude Hemorrhoidal Wipes
Active ingredientWITCH HAZEL
Label structure13 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

Storage: Store at room temperature.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel 25%

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

• 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

OTC - STOP USE SECTION

• Rectal bleeding occurs or;

• If condition worsens or does not improve within 7 days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

Storage

STORAGE AND HANDLING SECTION

Storage: Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions or Comments

OTC - QUESTIONS SECTION

1-877-432-4411

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dude Wipes 48Ct FilmDude Wipes 48Ct FilmDude Wipes Bundle FrontDude Wipes Bundle FrontDude Wipes Bundle BackDude Wipes Bundle BackBack Bundle LabelBack Bundle Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83731-05583731-055-48, 83731-055-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42025-10-03full-release2026-06-01 01:15:54

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dude Hemorrhoidal WipesWITCH HAZELDude Productsfdf408ef-9392-a812-e053-6394a90a00172026-08-25WarningsExact identifier
ndc (package): 83731-055-48
ndc (package): 83731-055-03
ndc (product): 83731-055
ndc11 (package): 83731005503
ndc11 (package): 83731005548
spl id: 59e03b68-3ac1-e933-e063-6294a90ac631
spl set id: fdf408ef-9392-a812-e053-6394a90a0017

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.