{De-Listing} LidoPatch (10882-526-30), 30 patch box, 3.6% lidocaine/1.25% menthol

LidoPatch by

Drug Labeling and Warnings

LidoPatch by is a Otc medication manufactured, distributed, or labeled by JAR Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LIDOPATCH- lidocaine, menthol patch 
JAR Laboratories

----------

{De-Listing} LidoPatch (10882-526-30), 30 patch box, 3.6% lidocaine/1.25% menthol

Active Ingredients

Lidocaine HCL 3.6%

Menthol 1.25%

Purpose

Topical Analgesic

Topical Analgesic

Temporarily relieves minor pain associated with: arthritis, simple backache, bursitis, tendonitis, muscle strains, sprains & bruises.


LidoPatch
contains lidocaine
PAIN RELIEF PATCH

For minor pain associated with
arthritis
back pain
muscle sprains & strains
The only over the counter patch with lidocaine
ultra thin, flexible, trim to fit

Warnings

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

Handling and Disposal

  • hands should be washed after the handling and eye contact should be avoided
  • do not store patch outside the sealed envelope
  • apply immediately after removal from protected envelope
  • fold used patches so that the adhesive side sticks to itself and safely discard used patches or pieces of cut patches where children and pets cannot get them
  • kept out of the reach of children both before and after use

Stop use and ask a doctor if

  • excessive redness or irritation is present
  • condition worsens
  • pain persists for more than 7 days
  • symptoms clear up and occur again within a few days

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

Directions

  • adults: apply patch to affected area for a maximum of 12 hours. Do not use more than 1 patch ever 24 hours.
  • children: consult your physician
  • remove protective film, gently apply to affected area

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

Inactive Ingredients

Dihydroxyaluminum Aminoscetate. Disodium EDTA, Glycerin, Methylparaben, Polysorbate 80, Polyvinyl alcohol, Propylene glycol, Propylparaben, Sodium, Carboxymethyl Cellulose, Sodium Polyacrylate, Tartaric acid, Titanium dioxide, Water

30ct box

LIDOPATCH 
lidocaine, menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 10882-526
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE505 mg
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL175 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: 10882-526-3030 in 1 BOX10/29/2015
11 in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/29/201511/01/2024
Labeler - JAR Laboratories (968952239)

Revised: 11/2025
 

Trademark Results [LidoPatch]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LIDOPATCH
LIDOPATCH
88345104 not registered Dead/Abandoned
J.A.R. Laboratories
2019-03-18
LIDOPATCH
LIDOPATCH
85324426 4077022 Dead/Cancelled
Ciullo, James J
2011-05-18

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.