NDC 11822-3627 Nicotine Transdermal


NDC Product Code 11822-3627

NDC CODE: 11822-3627

Proprietary Name: Nicotine Transdermal What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Nicotine What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication can help you quit smoking by replacing the nicotine in cigarettes. The nicotine in tobacco is an important part of cigarette addiction. When you stop smoking, your nicotine levels drop quickly. This drop can cause withdrawal symptoms such as craving tobacco, nervousness, irritability, headache, weight gain, and difficulty concentrating. Stopping smoking is hard and your chance of success is best when you are ready and have made a commitment to quit. Nicotine replacement products are part of a total stop-smoking program that includes behavior change, counseling, and support. Smoking causes lung disease, cancer, and heart disease. Stopping smoking is one of the most important things you can do to improve your health and live longer.

NDC Code Structure

  • 11822 - Rite Aid Corporation

NDC 11822-3627-3

Package Description: 56 PATCH in 1 CARTON > 1 KIT in 1 PATCH

NDC Product Information

Nicotine Transdermal with NDC 11822-3627 is a a human over the counter drug product labeled by Rite Aid Corporation. The generic name of Nicotine Transdermal is nicotine. The product's dosage form is kit and is administered via transdermal form.

Labeler Name: Rite Aid Corporation

Dosage Form: Kit - A packaged collection of related material.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.

Product Labeler Information

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

Labeler Name: Rite Aid Corporation
Labeler Code: 11822
FDA Application Number: NDA020076 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: NDA - A product marketed under an approved New Drug Application. 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.

Start Marketing Date: 03-31-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Nicotine Transdermal Product Label Images

Nicotine Transdermal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient Step 1 (In Each Patch)

Nicotine, 21 mg delivered over 24 hours

Active Ingredient Step 2 (In Each Patch)

Nicotine, 14 mg delivered over 24 hours

Active Ingredient Step 3 (In Each Patch)

Nicotine, 7 mg delivered over 24 hours


Stop smoking aid


Reduces withdrawal symptoms, including nicotine craving, associated with quitting smoking


If you are pregnant or breast-feeding, only use this medicine on the advice of your health care provider. Smoking can seriously harm your child. Try to stop smoking without using any nicotine replacement medicine. This medicine is believed to be safer than smoking. However, the risks to your child from this medicine are not fully known.

Do Not Use

  • •if you continue to smoke, chew tobacco, use snuff, use nicotine gum, or use another nicotine patch or other nicotine containing products

Ask A Doctor Before Use If You Have

  • •heart disease, recent heart attack, or irregular heartbeat. Nicotine can increase your heart rate. •high blood pressure not controlled with medication. Nicotine can increase your blood pressure. •an allergy to adhesive tape or have skin problems, because you are more likely to get rashes.

Ask A Doctor Or Pharmacist Before Use If You Are

  • •using a non-nicotine stop smoking drug •taking a prescription medicine for depression or asthma. Your prescription dose may need to be adjusted.

When Using This Product

  • •do not smoke even when not wearing the patch. The nicotine in your skin will still be entering your blood stream for several hours after you take off the patch. •if you have vivid dreams or other sleep disturbances remove this patch at bedtime

Stop Use And Ask A Doctor If

  • •skin redness caused by the patch does not go away after four days, or if your skin swells, or you get a rash •irregular heartbeat or palpitations occur •you get symptoms of nicotine overdose, such as nausea, vomiting, dizziness, weakness and rapid heartbeat

Keep Out Of Reach Of Children And Pets.

Used patches have enough nicotine to poison children and pets. If swallowed, get medical help or contact a Poison Control Center right away. Save pouch to use for patch disposal. Dispose of the used patches by folding sticky ends together and putting in pouch.


  • •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 •stop smoking completely when you begin using the patch •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 1-4Weeks 5-6Weeks 7-8 •if you smoke 10 or less cigarettes per day, start with Step 2 for 6 weeks, then Step 3 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 immediately press onto 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 same time each day •if you have vivid dreams, you may remove the patch at bedtime and apply a new one in the morning •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 it may irritate your skin and loses strength after 24 hours •to avoid possible burns, remove patch before undergoing any MRI (magnetic resonance imaging) procedures •stop using the patch at the end of 8 weeks. If you still feel the need to use the patch talk to your doctor.

Other Information

Store at 20-25°C (68-77°F)

Inactive Ingredients

Acrylate adhesive, aluminized polyester, cellulose paper, methacrylic acid copolymer

* Please review the disclaimer below.