LIDOCAINE PAIN RELIEF GEL-PATCH patch

Lidocaine Pain Relief Gel-Patch by

Drug Labeling and Warnings

Lidocaine Pain Relief Gel-Patch by is a Otc medication manufactured, distributed, or labeled by Dongguan Haiyi Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Lidocaine 4%

Inactive ingredients

Glycerin, Sodium Polyacrylate,Dihydroxyaluminum Aminoacetate,Disodium EthylenediaminetetraaceticAcid, Kaolin, Titanium Dioxide,Poly-sorbate 80, Propylene Glycol, TartaricAcid, Polyacrylic Acid,Polyvinylpyrroli-done K90, Methylparaben,Propylpara-ben, Water.

Purpose section

Desensitizes AggravatedNerves And Relieves Pain :

No lrritation

Stay-put Flexible Patch

Numbs Pain Away

Warning

For external use only

stop use

on wounds or damaged skin

with a heating pad or devic

with other ointments, creams,sprays, or liniments

if your are allergic to any ingredients of this product

not use

Not suitable for use by children, pregnantor breast feeding people.

Keep out of reach of children.

If swallowed accidentally , get medical help or contact with Poison Control Center immediately.

HOW TO USE

Adults and Children above 12 year sold:
Clean and dry the affected area.

Tear off the protective film andapply the exposed part of the patch tothe affected area.

Carefully remove remaining film while pressing the patch firmly on theskin.patch firmly on the skin.

Remove patch from the skin afterat most 8-hour application

Dosage

take an appropriateamount,Use 2-3 times a week

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIDOCAINE PAIN RELIEF GEL-PATCH 
lidocaine pain relief gel-patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-082
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
GLYCERIN (UNII: PDC6A3C0OX)
TARTARIC ACID (UNII: W4888I119H)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
POVIDONE K90 (UNII: RDH86HJV5Z)
METHYLPARABEN (UNII: A2I8C7HI9T)
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
KAOLIN (UNII: 24H4NWX5CO)
WATER (UNII: 059QF0KO0R)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-082-01	70 g in 1 BOX; Type 0: Not a Combination Product	11/04/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/04/2024

Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-082)