NDC 12823-401 Tenderwrap

NDC Product Code 12823-401

NDC CODE: 12823-401

Proprietary Name: Tenderwrap 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.

NDC Code Structure

NDC 12823-401-35

Package Description: 1 DRESSING in 1 BOX

NDC 12823-401-36

Package Description: 1 DRESSING in 1 BOX

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

NDC Product Information

Tenderwrap with NDC 12823-401 is a product labeled by Tyco Healthcare Group Lp. The product's dosage form is and is administered via form.

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.

  • ACACIA (UNII: 5C5403N26O)

Product Labeler Information

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

Labeler Name: Tyco Healthcare Group Lp
Labeler Code: 12823
Start Marketing Date: 07-29-2010 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: 12-31-2017 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.

Tenderwrap 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 Ingredients

Zinc Oxide 25%Calamine 1%


Skin Protectant


  • Dries the oozing and weeping of poison ivy, poison oak, or poison sumac.Ideal for the managing extremities (e.g. varicose ulcers) requiring protection and support.


  • Keep out of reach of children.For external use only.When using this product do not get into eyes.Stop use and ask a doctor if:                ● conditions worsens                ● symptoms last more than 7 days                ● clear up and occur again within a few days.


  • Begin bandaging at base of toes, without pressure, keeping foot and leg at right angle. Continue bandaging beyond ankle, doubling back to ensure molding to contours of the leg.Complete bandaging to just below the knee and apply an adhesive elastic bandage to secure the Unna Boot.Re-apply as needed

Other Ingredients

Acacia, Castor oil, Glycerin, and White Petrolatum.

* Please review the disclaimer below.