ELENZA PATCH- lidocaine hydrochloride and menthol patch 
Pharmaceutics Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Elenza Patch

Warnings

For external use only

Avoid contact with eyes

Do not applly to open wounds or damaged skin

If symptoms persist for more than seven days, discontinue use and consult physician

If swallowed, consult physician

Do not bandage tightly

If pregnant or breast feeding, contact physician prior to use

Do not use in large quantities, particularly over raw surfaces or blistered areas

Keep out of reach of children

Lidocaine HCL 4.00%

Menthol 1.00%

aloe barbadensis leaf, water, arnica montan extract, boswella serrata extract, camelia sinensis leaf extract, carbomer, ethylhexylglycerine, glycerine, isopropyl myristate, PEG 8, phenoxyethanol, polysorbate 80, sodium lauryl sulfate, triethanolamine, fd&c blue #1, fd&c yellow #5

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 consecutive days

children under 12 should consult physician prior to use

Temporary relief of pain associated with minor cuts, scrapes and minor skin irritations

Topical anesthetic

External analgesic

eLenza Patch

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ELENZA PATCH 
lidocaine hydrochloride patch
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:49430-017
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
MENTHOL (MENTHOL) MENTHOL1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
ARNICA MONTANA 
POLYSORBATE 80 
ALOE VERA LEAF 
BOSWELLIA SACRA WHOLE 
GREEN TEA LEAF 
CARBOMER 1342 
ETHYLHEXYLGLYCERIN 
ISOPROPYL MYRISTATE 
PEG-8 GLYCERYL ISOSTEARATE 
PHENOXYETHANOL 
SODIUM LAURYL SULFATE 
TRIETHANOLAMINE BENZOATE 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49430-017-15100 g in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/01/2013
Labeler - Pharmaceutics Corporation (079132026)
Establishment
NameAddressID/FEIBusiness Operations
Pure Source969241041manufacture(49430-017)

Revised: 9/2013
 
Pharmaceutics Corporation