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Lidozen

Dosage form: patch
Ingredients: LIDOCAINE HYDROCHLORIDE 40mg in 1g, MENTHOL, UNSPECIFIED FORM 10mg in 1g
Labeler: Proficient Rx LP
NDC code: 71205-302

Medically reviewed by Drugs.com. Last updated on Sep 21, 2023.

Lidozen Patch

DRUG FACTS:

ACTIVE INGREDIENTS:

Lidocaine HCL 4.00%

Menthol 1.00%

Toplcal Anesthetic

External Analgesic

USES:

For temporary relief of pain

WARNINGS:
For external use only.
Avoid contact with eyes.
If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.

Do not use 

in large quantities, particularly over raw surfaces or blistered areas.

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 right away.

DIRECTIONS (Adults and Children Over 12 Years):

Clean and dry affected area.

Remove patch from backing and apply to affected area.

Use only one patch at a time, and maximum of four patches / day.

Leave patch on affected area for up to 8 hours.

Do not use patches for longer than five consective days.

Children under 12 should consult physician prior to use.

INACTIVE INGREDIENTS:

Propylene Glycol, Carboxymethyl Cellulose Sodium, Dihydroxyaluminum Aminoacetate, Ethanol, Glycerin, Kaolin, Partially Neutralized Polyacrylate, Polysorbate 80, Polyvinylpyrrolidone 90, Tartaric Acid, Tetrasodium Edetate, Titanium Dioxide, Hydrogenated Castor Oil, Phenoxyethanol, Urea, Water.

Store below 25 degrees Celsius. Avoid directed sunlight.

Package Labeling:
LIDOZEN 
lidocaine hydrochloride, menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71205-302(NDC:71574-800)
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE40 mg  in 1 g
MENTHOL, UNSPECIFIED FORM (MENTHOL) MENTHOL, UNSPECIFIED FORM10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL 
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 
DIHYDROXYALUMINUM AMINOACETATE 
ALCOHOL 
GLYCERIN 
KAOLIN 
POLYSORBATE 80 
TARTARIC ACID 
EDETATE SODIUM 
TITANIUM DIOXIDE 
HYDROGENATED CASTOR OIL 
PHENOXYETHANOL 
UREA 
WATER 
Packaging
#Item CodePackage Description
1NDC:71205-302-055 PATCH in 1 POUCH
11 g in 1 PATCH
2NDC:71205-302-3030 PATCH in 1 POUCH
21 g in 1 PATCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/01/2019
Labeler - Proficient Rx LP (079196022)
Establishment
NameAddressID/FEIOperations
Proficient Rx LP079196022REPACK(71205-302), RELABEL(71205-302)

 
Proficient Rx LP

Further information

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