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:

when practical, clean the affected area with mild soap and warm water and rinse thoroughly
gently dry area by patting or blotting with toilet tissure or a soft cloth
pump a small amount of foam onto 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:

Bottle

THE PHARMA C COMPANY MEDICATED FOAM WITH WITCH HAZEL
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:55239-358
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:55239-358-00	210 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M015	05/15/2022

Labeler - Kleen Test Products Corporation (168165814)

The Pharma C Company Medicated Foam with Witch Hazel