LIDOPATCH PAIN RELIEF- lidocaine hcl, menthol patch 
JAR Laboratories

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LidoPatch (10882-529-01, 10882-529-03, 10882-529-30)

Active Ingredients

Lidocaine HCL 4%

Menthol 1%

Purpose

Topical Analgesic

Topical Analgesic

For temporary relief of pain.

Warnings

For external use only. Do not use if you are allergic or sensitive to lidocaine or menthol. Do not reuse, apply to intact skin only. Do not use if pouch is damaged or opened.

Handling and Disposal

Stop use and ask a doctor if

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

Directions

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

Inactive Ingredients

Dihydroxyaluminium Aminoacetate,Disodium EDTA,Glycerine ,Sopropyl Myristate, Methylparaben,Polysorbate 80,Polyvinyl Alcohol,Propylene Glycol,Propylparaben, Sodium Carboxymethyl Cellulose,Sodium Polyacrylate Tartaric Acid,Titanium Dioxide,
Water

Questions? Email support@lidopatch.com or call 866-284-2948

3ct box

label

outer box label

label 2

LIDOPATCH PAIN RELIEF 
lidocaine hcl, menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10882-529
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE100 mg
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL400 mg
Inactive Ingredients
Ingredient NameStrength
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
WATER (UNII: 059QF0KO0R)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
TARTARIC ACID (UNII: W4888I119H)  
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10882-529-011 in 1 BOX; Type 0: Not a Combination Product10/07/2023
2NDC:10882-529-033 in 1 BOX10/07/2023
21 in 1 PACKET; Type 0: Not a Combination Product
3NDC:10882-529-301 in 1 BOX10/07/2023
31 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/07/2023
Labeler - JAR Laboratories (968952239)

Revised: 10/2023
Document Id: 07289aba-63a2-a2c2-e063-6294a90ab1fa
Set id: 07289aa1-43ed-df31-e063-6394a90a764a
Version: 1
Effective Time: 20231007
 
JAR Laboratories