Pharma C wipes Hemorrhoidal

Manufacturer
Kleen Test Products Corporation
Effective date
2023-11-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:21:00

Label at a glance#

ProductPharma C wipes Hemorrhoidal
Active ingredientWITCH HAZEL
Label structure8 sections

Indications and uses

temporarily relieves the local itching and discomfort associated with hemorrhoids aids in protecting irritated anorectal areas temporarily relieves irritation and burning

Dosage and administration

Adults: Children under 12 years of age: ask a doctor 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 after application, discard pad and wash hands

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 the local itching and discomfort associated with hemorrhoids
  • aids in protecting irritated anorectal areas
  • temporarily relieves irritation and burning

Warnings

WARNINGS SECTION

For external use only.

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 or vagina by using fingers or mechanical device

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 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:

Children under 12 years of age: ask a doctor

  • 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
  • after application, discard pad and wash hands

Other information

SPL UNCLASSIFIED SECTION

Store at a controlled room temperature: 15-30°C (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Alcohol, Glycerin, Propanediol, Coco-Glucoside, Aloe Barbadensis Leaf Juice, Phenoxyethanol, Benzyl Alcohol, Potassium Sorbate, Tocopherol, Citric Acid, Sodium Citrate

Questions or comments?

OTC - QUESTIONS SECTION

1-844-308-8600

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55239-55555239-555-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
0a0aef1f-b991-0920-e063-6394a90aa146025c0c24-ac0f-42ed-a17c-fd70f1efd38a2023-11-13WarningsExact identifier
spl id: 0a0aef1f-b991-0920-e063-6394a90aa146
spl set id: 025c0c24-ac0f-42ed-a17c-fd70f1efd38a

Reported adverse events (FAERS/openFDA)#

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