Tucks

Manufacturer: Accupac LLC
Effective date: 2024-09-18
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:29:19

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 to 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

When using this product

OTC - WHEN USING SECTION

do not use more than directed unless told to do so by a doctor

do not put directly in the rectum by using fingers or any mechanical device or applicator

Stop use and ask 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 contact 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 to the affected area up to 6 times daily or after each bowel movement

Children under 12 years of age: ask a doctor

Other information

INFORMATION FOR PATIENTS 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 wipe in contact with 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

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1247709	Tucks 50 % Medicated Pad	PSN	2
844379	witch hazel 50 % Medicated Pad	PSN	2
1247709	witch hazel 500 MG/ML Medicated Pad [Tucks]	SBD	2
844379	witch hazel 500 MG/ML Medicated Pad	SCD	2
1247709	Tucks 50 % Medicated Pad	SY	2
1247709	Tucks 500 MG/ML Medicated Pad	SY	2
844379	witch hazel 50 % Medicated Pad	SY	2
844379	witch hazel 50 % Medicated Wipes	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
44038-0213-1	TucksMedicated Cooling Pads	1 in 1 CARTON	SOLUTION	1		2
44038-0213-1	TucksMedicated Cooling Pads	100 in 1 JAR	SOLUTION	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
44038-0213	TUCKS MEDICATED COOLING PADS (WITCH HAZEL) SOLUTION [ACCUPAC LLC]	2	2 package rows	20241027_227b652e-f251-9fac-e063-6294a90a8480.zip

Products#

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

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

Tucks Medicated Cooling Pads
Witch Hazel
SODIUM CITRATE, UNSPECIFIED FORM
EDETATE DISODIUM
CITRIC ACID MONOHYDRATE
PHENOXYETHANOL
WATER
ETHYLHEXYLGLYCERIN
POTASSIUM SORBATE
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
44038-0213	44038-0213-1

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
SODIUM CITRATE, UNSPECIFIED FORM	1Q73Q2JULR	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
WITCH HAZEL	101I4J0U34	ACTIB
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
WATER	059QF0KO0R	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
GLYCERIN	PDC6A3C0OX	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2268f3c7-014a-c025-e063-6294a90a5fb6			227b652e-f251-9fac-e063-6294a90a8480	2024-09-18	Warnings	Exact identifier spl id: 2268f3c7-014a-c025-e063-6294a90a5fb6 spl set id: 227b652e-f251-9fac-e063-6294a90a8480

Reported adverse events (FAERS/openFDA)#

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