FDA Label for Lidenza Patch
View Indications, Usage & Precautions
Lidenza Patch Product Label
The following document was submitted to the FDA by the labeler of this product Patchwerx Labs, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Otc - Active Ingredient
Lidocaine HCL 4.00%
Menthol 1.00%
Inactive Ingredient
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
Dosage & Administration
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
Indications & Usage
Temporary relief of pain associated with minor cuts, scrapes and minor skin irritations
Otc - Purpose
Topical anesthetic
External analgesic
* Please review the disclaimer below.