Label: LENZAPRO FLEX- lidocaine/menthol patch
- NDC Code(s): 70512-013-15
- Packager: SOLA Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 20, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENTActive ingredients: Lidocaine HCL 4% Menthol 4%
-
PURPOSEPurpose: Topical Anesthetic
-
INDICATIONS & USAGEUses: For the temporary relief of pain
-
WARNINGSWarnings: For external use
-
DO NOT USEDo not use: More than 1 patch on your body at a time or on cut, iritated or swollen skin. On puncture wounds - For more than 1 week without consulting a doctor
-
WHEN USINGWhen using this product: Use only as directed. Read and follow all directions and warnings on this label. Rare cases of serious burns have been reported with products of this type. Do not apply ...
-
STOP USEStop use and ask a doctor if: Condition worsens - Redness is present - Irritation developes - Symptoms persist for more than 7 days or clear up and occur again within a few days. You experience signs ...
-
PREGNANCY OR BREAST FEEDINGIf pregnant or breast-feeding, ask a health care professional before use.
-
KEEP OUT OF REACH OF CHILDRENKeep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.
-
DOSAGE & ADMINISTRATIONDirections: Adults and children over 12 years: Clean and dry the affected area. Open pouch and remove one patch. Remove the protective film from the patch and apply patch to the affected ...
-
OTHER SAFETY INFORMATIONOther Information: Avoid storing product in direct sunlight - Protect product from excessive mositure
-
INACTIVE INGREDIENTOther Ingredients: Acrylic Adhesive
-
PRINCIPAL DISPLAY PANELQuestions or comments? 866-747-7365 - Manufactured For: SOLA Pharmaceuticals LLC - Baton Rouge, LA 70810 - NDC: 70512-013-15 - QTY: 15 Articulated patches (5 per Resealable Pouch) x 3
-
INGREDIENTS AND APPEARANCEProduct Information