NDC 37205-739 Leader Medicated Pads

NDC Product Code 37205-739

NDC 37205-739-78

Package Description: 100 APPLICATOR in 1 JAR > 2.5 mL in 1 APPLICATOR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Leader Medicated Pads with NDC 37205-739 is product labeled by Cardinal Health. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Cardinal Health
Labeler Code: 37205
Start Marketing Date: 04-01-2012 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: 12-31-2018 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Leader Medicated Pads Product Label Images

Leader Medicated Pads 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

Otc - Active Ingredient

PurposeWitch Hazel 50%

Otc - Purpose

UsesTemporarily relieves these external symptoms associated with hemorrhoids:
itching, burning, and irritation


WarningsFor external use only.  Avoid contact with eyes.

Otc - When Using

  • When using this productDo not exceed the recommended daily dosage unless directed by a doctor
  • Do not put directly in rectum by using fingers or any mechanical
  • Device

Otc - Stop Use

  • Stop use and ask a doctor if Rectal bleeding occurs
  • Condition worsens or does not improve within 7 days

Otc - Keep Out Of Reach Of Children

Keep out of reach of childrenIf swallowed, get medical help or contact a Poison Control Center right

Indications & Usage

  • DirectionsAs hemorrhoidal treatment for adults:
  • 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 soft cloth before
  • Applying
  • Gently apply to the affected area by patting and then discard
  • Can be used up to six times daily or after each bowel movement
  • Children under 12 years of age: ask a doctor

Storage And Handling

Other informationStore at 20o to 25oC (68o to 77oF)

Inactive Ingredient

Inactive ingredients: alcohol, citric acid, diazolidinyl urea,
glycerin, methylparaben, propylene glycol, propylparaben, sodium citrate,

Dosage & Administration

DISTRIBUTED BY CARDINAL HEALTHDUBLIN, OHIO 43017CIN 1491687www.myleader.comMade in China

* Please review the disclaimer below.