Label: NWRB NICOTINE TRANSDERMAL PATCH- nicotine patch
- NDC Code(s): 84288-007-01
- Packager: Dongkou County Hecheng Network Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 2, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings 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.
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DO NOT USE
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
.Stomach ulcer or diabetes.
History of seizures
- WHEN USING
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STOP USE
Skin redness caused by the patch does not go away after four days, or if your skin swells,or you get a rash.
lrregular heartbeat or palpitations occur.
You get symptoms of nicotine overdose,such as nausea, vomiting, dizziness weakness, and rapid heartbeat.
You have symptoms of an allergic reaction(such as difficulty breathing or rash).
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
lf you are under 18 years of age, ask a doctor before use.
Before using this product, read the enclosed User's Guide for complete directions and other information.
Use 1 patch every 24 hours. Apply to a clean, dry,hairless area of skin on the upper arm, hip, or torso.
Begin using the patch on your quit day, use according to the following 8-week schedule.
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NWRB NICOTINE TRANSDERMAL PATCH
nicotine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84288-007 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 21 mg Inactive Ingredients Ingredient Name Strength LAURYL ALCOHOL (UNII: 178A96NLP2) POLYETHYLENE TEREPHTHALATE (INTRINSIC VISCOSITY 0.60-0.70) (UNII: 5YSH70HE6K) POLYACRYLATE-13 (UNII: FS2D4T67EA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84288-007-01 30 in 1 BOTTLE; Type 0: Not a Combination Product 12/02/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 12/02/2025 Labeler - Dongkou County Hecheng Network Technology Co., Ltd. (637818093) Establishment Name Address ID/FEI Business Operations Dongkou County Hecheng Network Technology Co., Ltd. 637818093 manufacture(84288-007)
