Label: SIELKIN QUIT SMOKING NICOTINE PATCHES- nicotine patch
- NDC Code(s): 83364-015-01
- Packager: YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 28, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
PRINCIPAL DISPLAY PANEL
Drug Facts

reduces withdrawal symptoms, including nicotine cravings associated with quitting smoking.
Ask a doctor before use if you have
■heart disease ■high blood pressure ■skin allergies ■diabetes ■history of seizuresAsk a doctor or pharmacist before use if you are■using a non-nicotine stop smoking drug■pregnant or breast-feeding
Directions
■ if you are under 18 years of age, ask a doctor before use.
■Before use, carefuly read the insert for complete instructions.
■lf you smoke more than 10 cigarettes per day, follow this 10-week schedule:Step 1 Step 2 Step 3
Cigarettes per Day
Week 1(Key Adjustment Phase) Weeks 2-6 Weeks 7-8 Weeks 9-10 10-20 cigarettes two 21mg patch/day one 21mg patch/day one 14mg patch/day one 7 mg patch/day 20+ cigarettes three 21mg patch/day two 21mg patch/day one 14mg patch/day one 7 mg patch/day ■lf you smoke 10 or fewer cigarettes per day, skip STEP 1(21mg). Start with STEP 2(14mg) for 6 weeks-using two14mg patches per day for the first week, then one 14mg patch per day for weeks 2 to 6. Then move to STEP 3(7mg) for 2weeks, and stop.
-
INGREDIENTS AND APPEARANCE
SIELKIN QUIT SMOKING NICOTINE PATCHES
nicotine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83364-015 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 7 mg in 1 g Inactive Ingredients Ingredient Name Strength BORNEOL (UNII: M89NIB437X) ALCOHOL (UNII: 3K9958V90M) METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13) ACRYLIC ACID (UNII: J94PBK7X8S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83364-015-01 30 in 1 BOX 01/01/2026 1 0.007 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2026 Labeler - YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD (725220463)
