Dude Hemorrhoidal Wipes

WITCH HAZEL TOPICAL HUMAN OTC DRUG

Dude Hemorrhoidal Wipes is an FDA drug label for the active ingredient WITCH HAZEL manufactured by Dude Products administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260825.

Generic name
WITCH HAZEL
Manufacturer
Dude Products
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
83731-055
Application
M015
Label effective
20260825

About this product

Dude Hemorrhoidal Wipes is an FDA-registered drug product whose active ingredient is WITCH HAZEL. It is labelled by Dude Products taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83731-055, application M015, label effective 20260825. It is one of 22 FDA drug label records sharing the active ingredient WITCH HAZEL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing WITCH HAZEL are most often described in connection with: temporarily relieves, external symptoms, hemorrhoids itching, burning irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Witch Hazel 25%

Indications & Usage

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

Dosage & Administration

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

More products with the same ingredient

WITCH HAZEL

DERLADIE MICELLAR CLEANSING WATER WITCH HAZEL

LAON COMMERCE co ltd View label

Equate Hemorrhoidal Medicated Wipes

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FAMILY Wellness MEDICATED HEMORRHOIDAL WIPES

Family Dollar Stores, Inc View label

Flushable Hemorrhoidal Medicated Wipes Maximum Strength

Amazon.com Services LLC View label

GNP Witch Hazel

Amerisource Bergen View label

Health Mart Witch Hazel

Strategic Sourcing Services LLC View label

Humco Witch Hazel

Humco Holding Group, Inc. View label

How products containing WITCH HAZEL compare

FDA lists 22 drug label records with WITCH HAZEL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Kleen Test Products Corporation 2
— — Strategic Sourcing Services LLC 2
— — ADUSA Distribution, LLC 1
— — Amazon.com Services LLC 1
— — Amerisource Bergen 1

Frequently asked questions

What is Dude Hemorrhoidal Wipes used for?
Uses • Temporarily relieves these external symptoms associated with hemorrhoids: • Itching • burning • irritation

Who makes Dude Hemorrhoidal Wipes?
Dude Products is the labeler of record for Dude Hemorrhoidal Wipes. 22 FDA label records share the active ingredient WITCH HAZEL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Dude Hemorrhoidal Wipes come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Dude Hemorrhoidal Wipes prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing WITCH HAZEL?
Yes. 22 FDA drug label records list WITCH HAZEL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Dude Hemorrhoidal Wipes been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.