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  4. NDC Product Code: 81799-001 Nicotine Transdermal Patches

NDC 81799-001 Nicotine Transdermal Patches

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81799-001?
  4. Nicotine Transdermal Patches 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 certification is expired.
NDC Product Code:
81799-001
Proprietary Name:
Nicotine Transdermal Patches
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Ehy Holdings Llc
Labeler Code:
81799
Product Label ID:
bf80e79b-f22f-5309-e053-2a95a90aee28
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
Code Structure:
Code Navigator:

Product Packages

NDC Code 81799-001-00

Package Description: 21 PATCH in 1 BOX / 21 mg in 1 PATCH

Product Details

What is NDC 81799-001?

The NDC code 81799-001 is assigned by the FDA to the product Nicotine Transdermal Patches which is product labeled by Ehy Holdings Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81799-001-00 21 patch in 1 box / 21 mg in 1 patch. 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 Nicotine Transdermal Patches?

*if you are under 18 years of age, ask a doctor before use.*before using this product, read the enclosed self-help guide for complete directions and other information *begin using the patch on your quit day *if you smoke more than 10 cigarettes per day, use the following schedule below： STEP 1STEP 2STEP 3Use one 21mg patch/dayUse one 14mg patch/dayUse one 7mg patch/dayWeeks 1-6Weeks 7-8Weeks 9-10*If you smoke 10 or less cigarettes per day, do not use Step 1(21mg) .Start with Step 2(14mg) for 6 weeks, then Step 3(7mg) for 2 weeks and then stop. *apply one new patch every 24 hours on skin that is dry, clean and hairless. *remove backing from patch and immed ately press on to skin.Hold for 10 seconds..wash hands after applying or removing patch. Save pouch to use for patch disposal.Dispose of the used patches by folding sticky ends together and putting in pouch. *the used patch should be removed and a new one applied to a different skin site at the sametime each day. *if you have vivid dreams, you may remove the patch at bedtime and apply a new one in the morning. *you may wear the patch for 18 to 24 hours *do not wear more than one patch at a time *do not cut patch in half or into smaller pieces *do not leave patch on for more than 24 hours because if may irritate your skin and loses strength after 24 hours *to avoid possible burns, remove patch before undergoing and MR(magnetic resonance imaging) procedures *it is important to complete treatment.If you feel you need to use the patch for a longer period to keep from smoking, talk to your healthcare provider.

Which are Nicotine Transdermal Patches UNII Codes?

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

Which are Nicotine Transdermal Patches 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:

* Please review the disclaimer below.

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".