PAIN RELIEVING GEL-PATCH- lidocaine patch 
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.

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Zeey, Pain Relieving Gel-Patch, Lidocaine 4%, N 5, N 15, N 18

Active ingredient

Lidocaine 4% ...... Purpose: Topical Anesthetic

Purpose

Topical Anesthetic

Uses

For temporary relief of pain

Warnings

For external use only

Ask a doctor if:

When using this product

Do not use

Stop use if:

Pregnancy or breast feeding

If pregnant or breastfeeding, ask a health professional before use

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adult and Children 12 years of age and over:

Children under 12 years of age: Consult a doctor

Dosage forms & strengths

This is a strip, patch dosage form.

The active ingredient strength is 4% w/w.

One patch one time, no more than 8 hours one time.

Inactive ingredients

Glycerin, Sodium Polyacrylate, Dihydroxyaluminum Aminoacetate, Disodium Ethylenediaminetetraacetic Acid, Kaolin, Titanium Dioxide, Polysorbate 80, Propylene Glycol, Tartaric Acid, Polyacrylic Acid, Polyvinylpyrrolidone K90, Methylparaben, Propylparaben, Water

Questions or Comments?

1 646-223-0128 · Lu.FDAmanage@gmail.com

Other information

Package label. Principal display panel

01051518

PAIN RELIEVING GEL-PATCH 
lidocaine patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73557-157
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE0.04 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
GLYCERIN (UNII: PDC6A3C0OX)  
POVIDONE K90 (UNII: RDH86HJV5Z)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
KAOLIN (UNII: 24H4NWX5CO)  
TARTARIC ACID (UNII: W4888I119H)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73557-157-055 in 1 BOX12/30/2022
1NDC:73557-157-0112 g in 1 PATCH; Type 0: Not a Combination Product
2NDC:73557-157-1515 in 1 BOX01/09/2024
2NDC:73557-157-0112 g in 1 PATCH; Type 0: Not a Combination Product
3NDC:73557-157-1818 in 1 BOX01/09/2024
3NDC:73557-157-0112 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/30/2022
Labeler - Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (546872672)
Registrant - Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (546872672)
Establishment
NameAddressID/FEIBusiness Operations
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.546872672manufacture(73557-157) , label(73557-157)

Revised: 4/2024
Document Id: 1738456d-6c25-fdd4-e063-6294a90aa630
Set id: f1045448-ae78-eba6-e053-2a95a90a6793
Version: 5
Effective Time: 20240429
 
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.