THE PHARMA C COMPANY TRIPLE ACTION HEMORRHOIDAL PADS- witch hazel, lidocaine, phenylephrine hydrochloride cloth 
Kleen Test Products Corporation

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The Pharma C Company Triple Action Hemorrhoidal Pads

Drug Facts

Active ingredients

Witch hazel (50% w/w)

Lidocaine (5%)

Phenylephrine HCl (0.25%)

Purpose

Hemorrhoidal astringent

Local anesthetic

Vasoconstrictor

Uses

Warnings

For external use only.

Ask a doctor before use if you have

• heart disease • high blood pressure • thyroid disease • diabetes • difficulty in urination due to enlargement of the prostate gland

Ask a doctor before use if you are

presently taking a prescription drug for high blood pressure or depression

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 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

Other information

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

Inactive ingredients

purified water, aloe barbadensis leaf juice, glycerin, propanediol, citric acid, phenoxyethanol, benzyl alcohol, potassium sorbate, tocopherol

Questions or comments?

1-844-308-8600

Package Labeling:

Label1

THE PHARMA C COMPANY TRIPLE ACTION HEMORRHOIDAL PADS 
witch hazel, lidocaine, phenylephrine hydrochloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55239-459
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL500 mg  in 1 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 g
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE2.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPANEDIOL (UNII: 5965N8W85T)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55239-459-00100 in 1 JAR01/15/2024
12 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01501/15/2024
Labeler - Kleen Test Products Corporation (168165814)

Revised: 2/2024
Document Id: 10dd13ca-98fc-5ccb-e063-6294a90a312d
Set id: ea090541-ab13-4ab0-9923-b97933b72766
Version: 1
Effective Time: 20240208
 
Kleen Test Products Corporation