Pharma C wipes Hemorrhoidal

Pharma C wipes Hemorrhoidal by

Drug Labeling and Warnings

Pharma C wipes Hemorrhoidal by is a Otc medication manufactured, distributed, or labeled by Kleen Test Products Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PHARMA C WIPES HEMORRHOIDAL- witch hazel cloth 
Kleen Test Products Corporation

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Pharma C wipes Hemorrhoidal

Drug Facts

Active ingredient

Witch Hazel (50%)

Purpose

Hemorrhoidal astringent

Uses

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

Warnings

For external use only.

When using this product

  • 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

rectal bleeding occurs condition worsens or does not improve within 7 days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

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

Inactive ingredients

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

Questions or comments?

1-844-308-8600

Package Labeling:

1

PHARMA C WIPES HEMORRHOIDAL 
witch hazel cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 55239-555
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL500 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPANEDIOL (UNII: 5965N8W85T)  
COCO GLUCOSIDE (UNII: ICS790225B)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
TOCOPHEROL (UNII: R0ZB2556P8)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 55239-555-01100 in 1 PACKAGE05/01/202112/01/2024
12 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01505/01/202112/01/2024
Labeler - Kleen Test Products Corporation (168165814)

Revised: 11/2023
Document Id: 0a0aef1f-b991-0920-e063-6394a90aa146
Set id: 025c0c24-ac0f-42ed-a17c-fd70f1efd38a
Version: 4
Effective Time: 20231113