HQLSEY QUIT SMOKING PATCHES- quit smoking patches patch

HQLSEY QUIT SMOKING PATCHES by

Drug Labeling and Warnings

HQLSEY QUIT SMOKING PATCHES by is a Otc medication manufactured, distributed, or labeled by Hansen Pharmaceutical Investment Co., Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Nicotine 21 mg/day

Purpose

Smoking cessation aid

Use

helps reduce withdrawal symptoms, including nicotine craving, associatedwith quitting smoking

Warnings

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

Do not use

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

Stop Use

skin irritation, redness, or swelling develops

Ask Doctor

If pregnant or breastfeeding,ask a doctor before use

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center right away

Directions

·if you smoke more than 10 cigarettes per day:
-use Step 1 (21 mg) patch for weeks 1-6
·apply one patch to a clean, dry, hairless area of skin on the upper body or outer part of the arm
·press patch frmly in place for about 10 seconds
·wash hands after applying or removing patch
·apply a new patch each day to a different area of skin
·do not use more than one patch at a time
·remove patch after 24 hours

Inactive ingredients

Acrylate copolymer adhesive, polyester backing film, release liner

Questions

For more information, please contact Hansen Pharmaceutical Investment Co. Ltd.
Address: RM507, 5/F, New East Ocean Centre,9 Science Museum Road,Tsim Sha Tsui East, Kowloon, Hong Kong

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HQLSEY QUIT SMOKING PATCHES 
quit smoking patches patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87405-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R)	NICOTINE	21 mg  in 100

Inactive Ingredients
Ingredient Name	Strength
ACRYLIC ACID (UNII: J94PBK7X8S)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
POLYESTER-7 (UNII: 0841698D2F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87405-001-01	14 in 1 BOX; Type 0: Not a Combination Product	02/25/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/25/2026

Labeler - Hansen Pharmaceutical Investment Co., Limited (687031012)

Establishment
Name	Address	ID/FEI	Business Operations
Hansen Pharmaceutical Investment Co., Limited		687031012	manufacture(87405-001)