Tucks Medicated Cooling Pads

Manufacturer
Blistex Inc | Accupac LLC
Effective date
2024-08-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:56:40

Label at a glance#

ProductTucks Medicated Cooling Pads
Active ingredientWITCH HAZEL
Label structure8 sections

Indications and uses

temporarily relieves the local itching and discomfort associated with hemorrhoids aids in protecting irritated ahorectal areas temporarily relieves irritation and burning

Dosage and administration

Adults: when practical, clean the affected area with mild soap and warm water, and rinse thoroughly gently dry by patting or blotting with toilet tissue or a soft cloth before applying apply externally fot the affected area up to 6 times daily or after each bowel movement Children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel (50% w/w)

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

temporarily relieves the local itching and discomfort associated with hemorrhoids

aids in protecting irritated ahorectal areas

temporarily relieves irritation and burning

Warnings

WARNINGS SECTION

For external use only

WARNINGS SECTION

Stop use and ask a doctor if

OTC - STOP USE SECTION

rectal bleeding occurs

condition worsens or does not improve within 7 days

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults:

when practical, clean the affected area with mild soap and warm water, and rinse thoroughly

gently dry by patting or blotting with toilet tissue or a soft cloth before applying

apply externally fot the affected area up to 6 times daily or after each bowel movement

Children under 12 years of age: ask a doctor

Other information

INSTRUCTIONS FOR USE SECTION

DO NOT FLUSH-after application, discard pad in trash and wash hands

for use as a moist compress--if necessary, first cleanse the area and place the wipe in contact with the irritated area for a soothing and cooling effect. Leave in place for up to 15 minutes and repeat as needed but not to exceed directions for use

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Glycerin

Sodium Citrate, Unspecified form

Citric Acid Monohydrate

Ethylhexylglycerin

Phenoxyethanol

Edetate Disodium

Potassium Sorbate

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-2103TUCKS MEDICATED COOLING PADS (WITCH HAZEL) SOLUTION [BLISTEX INC]1Current NDC, Legacy NDC20240816_1f40840d-2566-a77c-e063-6394a90ad494.zip

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
10157-210310157-2103-7

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

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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
486e2c85-fc93-2304-e063-6294a90a0ea11f40840d-2566-a77c-e063-6394a90ad4942026-01-15WarningsExact identifier
spl set id: 1f40840d-2566-a77c-e063-6394a90ad494
Tucks Medicated Cooling PadsWITCH HAZELBlistex Incb3e68008-3d0d-4124-9579-b503e9fb95c92024-12-13WarningsExact identifier
ndc (product): 10157-2103
Tucks Medicated Cooling PadsWITCH HAZELBlistex Inc1eb3c742-7104-7b47-e063-6394a90a84ba2024-08-02WarningsExact identifier
ndc (product): 10157-2103

Reported adverse events (FAERS/openFDA)#

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