DRAGON PAIN RELIEF- lidocaine patch 
Genomma Lab USA, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Dragon Pain Relief Patch Lidocaine 4% 5ct (224)

Active ingredient Purpose

Lidocaine 4%................................................................Topical anesthetic

Use

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

adults and children over 12 years:

children 12 years or younger: ask a doctor

Other information

store at room temperature 20-25°C (68-77°F)

Inactive ingredients

alcohol, aluminum glycinate, glycerin, kaolin, methylparaben, polysorbate 80, propylparaben, purified water, sodium polyacrylate, tartaric acid, titanium dioxide

Distributed by:

Genomma Lab USA, Inc.,

Houston, TX 77027

Made in China

224

DRAGON PAIN RELIEF 
lidocaine patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50066-224
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
GLYCERIN (UNII: PDC6A3C0OX)  
KAOLIN (UNII: 24H4NWX5CO)  
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)  
ALCOHOL (UNII: 3K9958V90M)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TARTARIC ACID (UNII: W4888I119H)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50066-224-055 in 1 CARTON01/18/2019
11 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/18/2019
Labeler - Genomma Lab USA, Inc. (832323534)

Revised: 3/2022
Document Id: db8af2b6-a822-2919-e053-2995a90a8729
Set id: 7fc18caf-cf4a-cdd0-e053-2991aa0a1be9
Version: 3
Effective Time: 20220331
 
Genomma Lab USA, Inc.