FDA.reportPublic FDA data

Flushable Hemorrhoidal Medical Wipes

Manufacturer
Kroger Company
Effective date
2020-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:38

Label at a glance#

ProductFlushable Hemorrhoidal Medical Wipes
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 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 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

OTHER SAFETY INFORMATION

Flush only one wipe at a time. Keep lid tightly closed when not in use.

Gently pull out wipe to dispense

Safe for well-maintained sewers and septic systems

Not recommended for use with basement pump systems

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 30142-314-48

COMPARE TO the active ingredient of PREPARATION H® MEDICATED WIPES

*See back panel

Kroger®

MAXIMUM STRENGTH

Flushable Hemorrhoidal Medicated Wipes

Witch Hazel, 50%

Gentle Everyday Cleansing to Reduce Irritation

With Aloe

PRE˜MOISTENED Cools, Soothes & Comforts Convenient, Easy to Use

48 MEDICATED WIPES 6.0 IN x 5.0 IN (15.2 cm x 12.7 cm)

LabelLabel

NDC 30142-314-96

COMPARE TO the active ingredient of PREPARATION H® MEDICATED WIPES

*See bottom panel

Kroger®

MAXIMUM STRENGTH

Flushable Hemorrhoidal Medicated Wipes

Witch Hazel, 50%

Gentle Everyday Cleansing to Reduce Irritation

With Aloe

PRE˜MOISTENED Cools, Soothes & Comforts Convenient, Easy to Use

2 X 48 CT PACKS

96 MEDICATED WIPES

Lable 1Lable 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
844379witch hazel 50 % Medicated PadPSN1
844379witch hazel 500 MG/ML Medicated PadSCD1
844379witch hazel 50 % Medicated PadSY1
844379witch hazel 50 % Medicated WipesSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
30142-314-482022-01-28C16284748780-1d6a99b39-d5d0-a426-e053-dadaa90af4c2Drug Facts
30142-314-962022-01-28C16284748780-1d6a99b39-d5d0-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-314-48Flushable Hemorrhoidal Medical Wipes48 in 1 BOXPATCH481
30142-314-48Flushable Hemorrhoidal Medical Wipes500 mg in 1 PATCHPATCH5001
30142-314-96Flushable Hemorrhoidal Medical Wipes96 in 1 BOXPATCH961
30142-314-96Flushable Hemorrhoidal Medical Wipes500 mg in 1 PATCHPATCH5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-314FLUSHABLE HEMORRHOIDAL MEDICAL WIPES (WITCH HAZEL) PATCH [KROGER COMPANY]1Legacy NDC, 4 package rows20200401_b3bc469e-15cc-4679-8ca9-01d77586473e.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30142-31430142-314-48, 30142-314-96

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
NameUNIIKind
WITCH HAZEL101I4J0U34ACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM CITRATE1Q73Q2JULRIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT

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
d2a1bb01-adba-4708-99bb-19875c52c7ceb3bc469e-15cc-4679-8ca9-01d77586473e2020-03-31WarningsExact identifier
spl id: d2a1bb01-adba-4708-99bb-19875c52c7ce
spl set id: b3bc469e-15cc-4679-8ca9-01d77586473e

Reported adverse events (FAERS/openFDA)#

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