Natural health product · DIN 02065754
Nicorette Patch 10mg
No: licence discontinued
The licence holder discontinued the product licence.
Licence status Discontinued; licensed November 20, 2009; licence last revised August 13, 2010.
- DIN
- 02065754
- Licence holder
- McNeil Consumer Healthcare, division of Johnson & Johnson Inc.Markham, Ontario, Canada
- Dosage form
- Patch
- Route
- Transdermal
- Licensing route
- Transitional DIN
- First licensed
- November 20, 2009
- Licence last revised
- August 13, 2010
Also sold as
Other product names on the same licence.
- Nicorette® ComboQuit¿
Medicinal ingredients
Per dosage unit, as licensed.
| Ingredient | Amount | Source and potency |
|---|---|---|
| (S)-3-(1-methyl -2-pyrrolidinyl)pyridine | 16.6 mg | Nicotina tobaccum |
What it is licensed for
The licence’s own wording. Directions, doses, cautions and warnings are on the official record and the label.
- Increase your chances. NICORETTE Patch 10 mg/16hr offers controlled-release nicotine throughout the day to reduce withdrawal symptoms and nicotine cravings. To increase your chance of quitting use with a stop smoking support program. Combination treatment: If you have relapsed or if you have had tough/intense cravings while using the patch alone, now you can use the patch in combination with NICORETTE 2 mg gum for better craving relief. Combination treatment: Use the patch as directed and chew 5-6 pieces of gum per day (maximum 15 pieces per day).
Non-medicinal ingredients
Polyisobutylene; Polybutene; Polyester