FDA.reportPublic FDA data

Maximum Strength Hemorrhoidal Pads

Manufacturer
Walmart, Inc.
Effective date
2025-07-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:07:17

Label at a glance#

ProductMaximum Strength Hemorrhoidal Pads
Active ingredientWITCH HAZEL
Label structure9 sections

Indications and uses

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

Dosage and administration

As hemorrhoidal treatment for adults: when practial 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 15 0 - 30 o C (59 0 - 86 o F)

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 any mechanical device.

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 reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center right away. (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

As hemorrhoidal treatment for adults:

  • when practial 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 15 0- 30 oC (59 0- 86 oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Citrate, Citric Acid, Glycerin, Phenoxyethanol, Potassium Sorbate.

Questions or Comments?

OTC - QUESTIONS SECTION

Satisfaction Guaranteed - Or we'll replace it Or give you your money back. For questions or comment or to report an undesired reaction or side effect please call 1-888-287-1915

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49035-465-10

equate TM

Maximum Strength Hemorrhoidal Pads

Compare to the active ingredient in TUCKS ®Medicated Pads*

Medicated cool relief with witch hazel soothes and provides temporary relief of hemorrhoidal irritation and burning

  • For use with hemorrhoids and vaginal care
  • Protects irritated areas
  • Convenient and easy to use

100 PADS

LabelLabel

NDC 49035-465-20

equate TM

Maximum Strength Hemorrhoidal Pads

Compare to the active ingredient in TUCKS® Medicated Pads*

Medicated cool relief with witch hazel soothes and provides temporary relief of hemorrhoidal irritation and burning

  • For use with hemorrhoids and vaginal care
  • Protects irritated areas
  • Convenient and easy to use

200 PADS

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
844379witch hazel 50 % Medicated PadPSN3
844379witch hazel 500 MG/ML Medicated PadSCD3
844379witch hazel 50 % Medicated PadSY3
844379witch hazel 50 % Medicated WipesSY3

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
49035-465-102024-12-20C16284748780-1ba0f9c33-3066-a910-e053-dadaa90a0b85Drug Facts
49035-465-202024-12-20C16284748780-1ba0f9c33-3066-a910-e053-dadaa90a0b85Drug Facts
49035-465-102021-01-29C16284748780-1ba0f9c33-3066-a910-e053-dadaa90a0b85Drug Facts
49035-465-202021-01-29C16284748780-1ba0f9c33-3066-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-465-10Maximum Strength Hemorrhoidal Pads100 in 1 JARCLOTH1003
49035-465-20Maximum Strength Hemorrhoidal Pads200 in 1 JARCLOTH2003

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
49035-46549035-465-10, 49035-465-20

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
Maximum Strength Hemorrhoidal PadsWITCH HAZELWalmart, Inc.6dd8d3d9-5109-4869-917b-9521e9ba1ed02025-07-14WarningsExact identifier
ndc (package): 49035-465-10
ndc (package): 49035-465-20
ndc (product): 49035-465
ndc11 (package): 49035046520
ndc11 (package): 49035046510
spl id: 39e9aa87-d355-96dc-e063-6294a90a1c4b
spl set id: 6dd8d3d9-5109-4869-917b-9521e9ba1ed0

Reported adverse events (FAERS/openFDA)#

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