NDC 55239-555 Pharma C Wipes Hemorrhoidal

Witch Hazel

NDC Product Code 55239-555

NDC 55239-555-01

Package Description: 100 PATCH in 1 PACKAGE > 2 mL in 1 PATCH

NDC Product Information

Pharma C Wipes Hemorrhoidal with NDC 55239-555 is a a human over the counter drug product labeled by Kleen Test Products Corporation. The generic name of Pharma C Wipes Hemorrhoidal is witch hazel. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Kleen Test Products Corporation

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Pharma C Wipes Hemorrhoidal Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • WITCH HAZEL 500 mg/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • 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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Kleen Test Products Corporation
Labeler Code: 55239
FDA Application Number: part346 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-01-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Pharma C Wipes Hemorrhoidal Product Label Images

Pharma C Wipes Hemorrhoidal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Witch Hazel (50%)

Purpose

Hemorrhoidal astringent

Uses

  • Temporarily relieves the local itching and discomfort associated with hemorrhoidsaids in protecting irritated anorectal areastemporarily 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 doctordo 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 thoroughlygently dry by patting or blotting with toilet tissue or a soft cloth before applyingapply externally to the affected area up to 6 times daily or after each bowel movementafter application, discard pad and wash handsChildren under 12 years of age: ask a doctor

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

* Please review the disclaimer below.