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

The Pharma C Company Medicated Foam with Witch Hazel by

Drug Labeling and Warnings

The Pharma C Company 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]

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:

INGREDIENTS AND APPEARANCE

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

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

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

Labeler - Kleen Test Products Corporation (168165814)