NDC 37205-739 Leader Medicated Pads

  1. Labeler Index
  2. Cardinal Health
  3. NDC: 37205-739 Leader Medicated Pads

NDC Product Code 37205-739

NDC CODE: 37205-739

Proprietary Name: Leader Medicated Pads What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as usestemporarily relieves these external symptoms associated with hemorrhoids: itching, burning, and irritation

NDC Code Structure

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)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • 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

Active
ingredient                                                                
PurposeWitch Hazel 50%
...............................................................Astringent

Otc - Purpose

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

Warnings

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
away.

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,
water

Dosage & Administration

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

* Please review the disclaimer below.