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  4. NDC Product Code: 69329-260 Dermawerx Surgical Prepak

NDC 69329-260 Dermawerx Surgical Prepak

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69329-260?
  4. Dermawerx Surgical Prepak Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69329-260
Proprietary Name:
Dermawerx Surgical Prepak
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Patchwerx Labs, Inc.
Labeler Code:
69329
Product Label ID:
2687330c-50dc-0339-e054-00144ff88e88
Start Marketing Date: [9]
12-10-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69329-260?

The NDC code 69329-260 is assigned by the FDA to the product Dermawerx Surgical Prepak which is product labeled by Patchwerx Labs, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69329-260-01 1 kit in 1 kit * 237 ml in 1 bottle, plastic (0116-1061-08) * 118 ml in 1 tube (69329-253-02). 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 Dermawerx Surgical Prepak?

Use with care in premature infants and infants under 2 months of age. These products may cause irritation or chemical burns.Surgical hand scrub:wet hands and forearms with waterscrub for 3 minutes with about 5 ml of product and a wet brush paying close attention to the nails, cuticles and interdigital spacesa separate nail cleaner may be usedrinse thoroughlywash for an additional 3 minutes with 5 ml of product and rinse under running waterdry thoroughlyHealthcare personnel handwash:wet hands with waterdispense about 5 ml of product into cupped hands and wash in a vigorous manner for 15 secondsrinse and dry thoroughlyPatient preoperative skin preparation:apply product liberally to surgical site and swab for at least 2 minutes and dry with a sterile towelrepeat procedure for an additional 2 minutes and dry with a sterile towelSkin wound and general skin cleaning:thoroughly rinse the area to be cleaned with waterapply the minimum amount of product necessary to cover the skin or wound area and wash gentlyrinse again thoroughly gently cleanse and dry affected areaapply liberally to affected area as needed.

Which are Dermawerx Surgical Prepak UNII Codes?

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

Which are Dermawerx Surgical Prepak 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:

What is the NDC to RxNorm Crosswalk for Dermawerx Surgical Prepak?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".