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  4. NDC Product Code: 59229-001 Bandage

NDC 59229-001 Bandage

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59229-001?
  4. Bandage Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59229-001
Proprietary Name:
Bandage
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yuyao Chengze Medical Supplies Factory
Labeler Code:
59229
Product Label ID:
d2dabc21-f9c7-4d16-8066-976033f74505
Start Marketing Date: [9]
07-06-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59229-001-01

Package Description: 24 BOX in 1 CARTON / 40 POUCH in 1 BOX / .0459 mg in 1 POUCH

NDC Code 59229-001-02

Package Description: 36 BOX in 1 CARTON / 40 POUCH in 1 BOX / .0459 mg in 1 POUCH

Product Details

What is NDC 59229-001?

The NDC code 59229-001 is assigned by the FDA to the product Bandage which is product labeled by Yuyao Chengze Medical Supplies Factory. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 59229-001-01 24 box in 1 carton / 40 pouch in 1 box / .0459 mg in 1 pouch, 59229-001-02 36 box in 1 carton / 40 pouch in 1 box / .0459 mg in 1 pouch. 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 Bandage?

Clean and dry the affected area .Apply a sterile bandage on the area 1 to 3 times daily.Other information :not intended for use on delicate or sensitive skin.

Which are Bandage UNII Codes?

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

Which are Bandage 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".