Skip to main content

Lidopatch

Medically reviewed by Drugs.com. Last updated on Nov 8, 2021.

Dosage form: patch
Ingredients: LIDOCAINE 0.036mg, MENTHOL 0.0125mg
Labeler: J.A.R. Laboratories
NDC Code: 10882-527

Lidopatch

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

PURPOSE

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


ACTIVE INGREDIENT SECTION
Lidocaine HCL 3.6% - Topical analgesic
Menthol 1.25% - Topical analgesic

STOP USE SECTION
Stop Use and ask doctor if:
excessive redness or irritation is present
Pain persists for more than 7 days
symptoms cear up and occur again within a few days
conditions worsens
If pregnant or breasfeading, ask a health professional before use. keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION


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

INACTIVE INGREDIENT SECTION


Dihydroxyaluminum aminoacetate, Disodium EDTA, Glycerine, Methylparaben, Polysorbate 80, Polyvinyl alcohol, Propylene glycol, Propyl paraben, Sodium, Carboxymethylcellulose, Sodium Polyacrylate, Tartaric acid, Titanium dioxide, Water

Usage
Aduts apply patch to affected area for a maximum of 12 hours.
Do not use more than 1 patch every 24 hours

KEEP OUT OF REACH OF CHILDREN.

PACKAGE LABEL

LIDOPATCH 
lidocaine, menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10882-527
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (LIDOCAINE) LIDOCAINE0.036 mg
MENTHOL (MENTHOL) MENTHOL0.0125 mg
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
PROPYLPARABEN 
SODIUM POLYACRYLATE (8000 MW) 
POLYVINYL ALCOHOL, UNSPECIFIED 
CARBOXYMETHYLCELLULOSE 
GLYCERIN 
POLYSORBATE 80 
DIHYDROXYALUMINUM AMINOACETATE 
EDETATE DISODIUM ANHYDROUS 
METHYLPARABEN 
TARTARIC ACID 
TITANIUM DIOXIDE 
ISOPROPYL MYRISTATE 
Packaging
#Item CodePackage Description
1NDC:10882-527-011 PATCH in 1 PACKAGE
2NDC:10882-527-0230 PATCH in 1 PACKAGE
3NDC:10882-527-0430 PATCH in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/02/2016
Labeler - J.A.R. Laboratories (968952239)
Establishment
NameAddressID/FEIOperations
Bingbing Pharmaceutical (Hubei) Co., Ltd554413454manufacture(10882-527)
Establishment
NameAddressID/FEIOperations
INTERMED676244169manufacture(10882-527)

 
J.A.R. Laboratories

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.