Meicated Wipe

Manufacturer
Diamond Wipes International, Inc
Effective date
2025-11-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:17:47

Label at a glance#

ProductMeicated Wipe
Active ingredientWITCH HAZEL
Label structure8 sections

Indications and uses

■Temporarily relieves itching, burning, and irritation associated with hemorrhoids. ■Gently cleanses and soothes the affected area.

Dosage and administration

■ Open the label of the wipes pouch. Gtab the wipe and pull out of pouch. ■ Keep package tightly closed to retain moisture. ■ Adults: Cleanse the affected area with a wipe by gently patting, then discard. ■ Use up to 6 times daily or after each bowel movement. ■ Do not flush more than one wipe at a time. ■ Children under 12: Ask a doctor before use. ■ Store at room temperature.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel, 50%

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

■Temporarily relieves itching, burning, and irritation associated with hemorrhoids.

■Gently cleanses and soothes the affected area.

Warnings

WARNINGS SECTION

For external use only. Do not use if allergic to any of the ingredients

When using this product

■ Do not insert into the rectum using fingers or any device. or applicator.

■ Do not apply to open wounds or damaged skin.

Stop use and ask a doctor if

■ Condition worsens or does not improve within 7 days.

■ Bleeding occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Open the label of the wipes pouch. Gtab the wipe and pull out of pouch.

■ Keep package tightly closed to retain moisture.

■ Adults: Cleanse the affected area with a wipe by gently patting, then discard.

■ Use up to 6 times daily or after each bowel movement.

■ Do not flush more than one wipe at a time.

■ Children under 12: Ask a doctor before use.

■ Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citric Acid, Cocamidopropyl Betaine, Diazolidinyl Urea, Glycerin, Methylparaben, Propylene Glycol, Sodium Citrate, Water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TENDER TOUCH BY Diamond Wipes®

MEDICATED HEMORRHOIDAL WIPES

PEEL HERE

Hemorrhoidal Care

Vaginal Care

Witch Hazel

Aloe Vera

Soothing

FLUSHABLE

48 WIPES

6x5in

LABELLABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
844379witch hazel 50 % Medicated PadPSN1
844379witch hazel 500 MG/ML Medicated PadSCD1
844379witch hazel 50 % Medicated PadSY1
844379witch hazel 50 % Medicated WipesSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64709-120-01Meicated Wipe195.09 g in 1 POUCHCLOTH195.091

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64709-12064709-120-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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
Meicated WipeWITCH HAZELDiamond Wipes International, Inc4458c80c-d013-55ba-e063-6394a90a6b392025-11-24WarningsExact identifier
ndc (package): 64709-120-01
ndc (product): 64709-120
ndc11 (package): 64709012001
spl id: 4458c70d-0eec-02a5-e063-6294a90a5242
spl set id: 4458c80c-d013-55ba-e063-6394a90a6b39

Reported adverse events (FAERS/openFDA)#

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