medicated pads

Manufacturer: TARGET CORPORATION
Effective date: 2025-10-14
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 01:38:58

Label at a glance#

Productmedicated pads

Active ingredientWITCH HAZEL

Label structure8 sections

Indications and uses

Temporarily relieves these external symptoms associated with hemorrhoids: itching burning irritation

Dosage and administration

As 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. can be used up to six times daily or after each bowel movement. Children under 12 years of age consult a doctor.

Storage and handling

Store at controlled room temperature: 15º-30ºC (59º-86ºF)

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel 50%

Purpose

OTC - PURPOSE SECTION

Hemorrhoidal 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 into rectum or vagina using fingers or mechanical device.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

rectal bleeding occurs
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 at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

As 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.
can be used up to six times daily or after each bowel movement.

Children under 12 years of age

consult a doctor.

Other Information

STORAGE AND HANDLING SECTION

Store at controlled room temperature: 15º-30ºC (59º-86ºF)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Extract, Sodium Citrate, Citric Acid, Glycerin, Phenoxyethanol, Potassium Sorbate

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 11673-614-10

Compare to Tucks ^®*

medicated pads

cooling hemmorhoidal relief

soothing witch hazel helps protect irritated areas

pH balanced

100 PADS

3 IN X 3 IN (7.6 cm X 7.6 cm)

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
844379	witch hazel 50 % Medicated Pad	PSN	6
844379	witch hazel 500 MG/ML Medicated Pad	SCD	6
844379	witch hazel 50 % Medicated Pad	SY	6
844379	witch hazel 50 % Medicated Wipes	SY	6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11673-614-10	2022-01-28	C162847	48780-1	d6a99b39-334d-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11673-614-10	medicated pads	100 in 1 BOX	PATCH	100		6
11673-614-10	medicated pads	50 mg in 1 PATCH	PATCH	50		6

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

medicated pads
Witch Hazel
WATER
ALOE VERA LEAF
SODIUM CITRATE
CITRIC ACID MONOHYDRATE
GLYCERIN
PHENOXYETHANOL
POTASSIUM SORBATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11673-614	11673-614-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
GLYCERIN	PDC6A3C0OX	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
WITCH HAZEL	101I4J0U34	ACTIB

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
medicated pads	WITCH HAZEL	TARGET CORPORATION	acd0d99d-2a77-4227-bebb-c819f4a52666	2025-10-14	Warnings	Exact identifier ndc (package): 11673-614-10 ndc (product): 11673-614 ndc11 (package): 11673061410 spl id: 412203ce-d7fc-28ee-e063-6394a90a929f spl set id: acd0d99d-2a77-4227-bebb-c819f4a52666

Reported adverse events (FAERS/openFDA)#

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