PHARMA C WIPES HEMORRHOIDAL- witch hazel cloth

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]

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:

INGREDIENTS AND APPEARANCE

PHARMA C WIPES HEMORRHOIDAL 
witch hazel cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55239-555
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	500 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55239-555-01	100 in 1 PACKAGE	05/01/2021	12/01/2024
1		2 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	05/01/2021	12/01/2024

Labeler - Kleen Test Products Corporation (168165814)