FDA.reportPublic FDA data

hemorrhoidal pads

Manufacturer
Meijer Distribution Inc.
Effective date
2025-07-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:07:16

Label at a glance#

Producthemorrhoidal pads
Active ingredientWITCH HAZEL
Label structure10 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)

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 rectal 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, Sodium citrate, Citric acid, Glycerin, Phenoxyethanol, Potassium sorbate

OTHER SAFETY INFORMATION

Do not use this product if seal on jar is broken or missing.

SPL UNCLASSIFIED SECTION

* This product is not manufactured or distributed by Blistex, Inc., owner of the registered trademark TUCKS®.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 41250-868-10

meijer

Compare to Tucks

hemorrhoidal pads

Medicated Cool Relief with Witch Hazel

MAXIMUM STRENGTH

100 PADS 3 IN DIA (7.62 cm DIA)

DO NOT FLUSH

100100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
844379witch hazel 50 % Medicated PadPSN4
844379witch hazel 500 MG/ML Medicated PadSCD4
844379witch hazel 50 % Medicated PadSY4
844379witch hazel 50 % Medicated WipesSY4

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41250-868-102022-12-19C16284748780-1ba0f9c33-3d98-a910-e053-dadaa90a0b85Drug Facts
41250-868-102021-01-29C16284748780-1ba0f9c33-3d98-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-868-10hemorrhoidal pads100 in 1 BOXPATCH1004
41250-868-10hemorrhoidal pads500 mg in 1 PATCHPATCH5004

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-86841250-868-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM CITRATE1Q73Q2JULRIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WITCH HAZEL101I4J0U34ACTIB

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
hemorrhoidal padsWITCH HAZELMeijer Distribution Inc.53e39d22-a89e-4f95-8c64-abeb50f72ce72025-07-11WarningsExact identifier
ndc (package): 41250-868-10
ndc (product): 41250-868
ndc11 (package): 41250086810
spl id: 39ad74f5-b6ff-96bf-e063-6394a90a3585
spl set id: 53e39d22-a89e-4f95-8c64-abeb50f72ce7

Reported adverse events (FAERS/openFDA)#

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