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NDC 71149-0001 Mousturizing Gloves And Socks

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71149-0001?
  4. Mousturizing Gloves And Socks 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.

Get all the details for National Drug Code (NDC) 71149-0001 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
71149-0001
Proprietary Name:
Mousturizing Gloves And Socks
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Clean Sense
Labeler Code:
71149
Product Label ID:
44b29200-8560-0405-e054-00144ff8d46c
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
12-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 71149-0001?

The NDC code 71149-0001 is assigned by the FDA to the product Mousturizing Gloves And Socks which is product labeled by Clean Sense. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71149-0001-1 6 g 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 Mousturizing Gloves And Socks?

Moisturizing Socks 1. Rinse feet thoroughly and completely dry them to remove any moisture. 2. Insert feet in the moisturizing socks and make sure the contents of the liquid are inside. 3. While wearing the moisturizing socks, massage feet to absorb all the liquid. 4. After 20 to 30 minutes, remove moisturizing socks and massage in the remaining liquid for long-lasting hydration. Moisturizing Gloves 1. Wash hands thoroughly and completely dry them to remove any moisture. 2. Open and put hands in the hand moisturizing treatment and make sure the contents of the liquid makeup is inside. 3. While wearing the hand moisturizing treatment, massage them to thoroughly absorb all the moisture. 4. After 20-30 minutes remove the hand moisturizing treatment and softly pat down the remaining contents for better absorption.

Which are Mousturizing Gloves And Socks UNII Codes?

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

Which are Mousturizing Gloves And Socks 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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".