NDC 68345-272 Repara

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68345-272
Proprietary Name:
Repara
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pss World Medical, Inc.
Labeler Code:
68345
Start Marketing Date: [9]
05-17-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68345-272-01

Package Description: 1 DRESSING in 1 BOX

NDC Code 68345-272-02

Package Description: 1 DRESSING in 1 BOX

Product Details

What is NDC 68345-272?

The NDC code 68345-272 is assigned by the FDA to the product Repara which is product labeled by Pss World Medical, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 68345-272-01 1 dressing in 1 box , 68345-272-02 1 dressing in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Repara?

Apply as neededCleanse the leg and dry the skin.If a wound is present, apply an appropriate wound dressing for moist wound healing.With a foot positioned at 90o or right angle to the leg (dorsiflexed) begin wrapping the medicated bandage without tension beginning at the base of the toes. Wrap the leg without tension overlapping each layer by 50% or half the width of the dressing. Smooth and mold the bandage while wrapping.Wrap all the way up the leg stopping one finger width below the posterior knee.Apply an elastic adhesive bandage (not included), following the manufacturer's instructions.

Which are Repara UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Repara Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".