Pharma C Wipes Medicated Foam with Witch Hazel

Pharma C Wipes Medicated Foam with Witch Hazel by

Drug Labeling and Warnings

Pharma C Wipes Medicated Foam with Witch Hazel 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 MEDICATED FOAM WITH WITCH HAZEL- witch hazel liquid 
Kleen Test Products Corporation

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Pharma C Wipes Medicated Foam with Witch Hazel

Drug Facts

Active ingredient

Witch hazel 50%

Purpose

Hemorrhoidal astringent

Uses

tempoDirectionsrarily 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: when practical, clean the affected area with mild soap and warm water and rinse thoroughly gently dry area by patting or blotting with toilet tissue or a soft cloth apply a small amount of foam to clean toilet paper and apply externally to the affected area after application, flush toilet paper and wash hands medicated foam may be used up to 6 times daily or after each bowel movement Children under 12 years of age: ask a doctor




Other information

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

Inactive ingredients

aloe barbadensis leaf juice, benzyl alcohol, citric acid, coco-glucoside, ethyl alcohol, glycerin, phenoxyethanol, potassium sorbate, propanediol, purified water, sodium citrate, tocopherol

Questions or comments?

1-844-308-8600

Package Labeling:

Label

PHARMA C WIPES MEDICATED FOAM WITH WITCH HAZEL 
witch hazel liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 55239-357
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCO GLUCOSIDE (UNII: ICS790225B)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPANEDIOL (UNII: 5965N8W85T)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 55239-357-00210 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/202212/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01504/15/202212/31/2023
Labeler - Kleen Test Products Corporation (168165814)
Establishment
NameAddressID/FEIBusiness Operations
Kleen Test Products Corporation168165814manufacture(55239-357)

Revised: 11/2023
Document Id: 0a096ef2-acd6-99f2-e063-6294a90a4f97
Set id: f1dd7380-1835-4907-9e5b-459f3f94f132
Version: 3
Effective Time: 20231113