LenzaPatch by Pharmaceutica North America, Inc.
Dosage form: liquid
Ingredients: LIDOCAINE HYDROCHLORIDE 4g in 100g, MENTHOL 1g in 100g
Labeler: Pharmaceutica North America, Inc.
NDC Code: 45861-017
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Lidocaine HCL 4.00%
Menthol 1.00%
Topical Analgesic
External Analgesic
For temporary relief of pain associated with minor cuts, scrapes and minor skin irritations.
- For external use only
- Avoid contact with eyes
- Do not apply 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.
- 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.
Aloe Barbadensis Leaf (Aloe Vera Juice) Gel, Aqua (Deionized Water), Arnica Montana Extract, Boswellia Serrata Extract, Camellia Sinensis Leaf (Green Tea) Extract, Carbomer, Ethylhexylglycerin, Glycerin, Isopropyl Myristate, PEG-8, Phenoxyethanol, Polysorbate-80, Sodium Lauryl Sulfate, Triethanolamine, FD C Blue 1, FD C Yellow 5.
| LENZAPATCH
lidocaine hydrochloride, menthol liquid |
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| Labeler - Pharmaceutica North America, Inc. (962739699) |
Medically reviewed on Dec 17, 2018
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
