eLenza Patch description, usages, side effects, indications, overdosage, supplying and lots more!

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eLenza Patch

Pharmaceutics Corporation

Elenza Patch


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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

Active ingredient

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

Uses

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

Purpose

Topical anesthetic

External analgesic

eLenza Patch

eLenza Patch

eLenza Patch

Lidocaine Hydrochloride PATCH

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49430-017
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE LIDOCAINE 4 g
MENTHOL 1 g

Inactive Ingredients

Ingredient Name Strength
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:49430-017-15 100 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-10-01


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Be sure to consult your doctor before taking any medication!
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