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 a product labeled by Cardinal Health. The generic name of Leader Medicated Pads is . The product's dosage form is and is administered via form.

Labeler Name: Cardinal Health

Dosage Form: -

Product Type: 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.

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 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. Values = ‘Y’ or ‘N’.

* 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.