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 December 8, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
-
WHEN USING
When 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 to wounds or damaged, broken or irritated skin.
- Do not allow contact with the eyes and mucous membranes.
- Do not bandage tightly or apply local heat (such as heating pads) to the area of use.
- Do not use at the same time as other topical analgesics.
- Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions:
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 area.
- Reseal pouch containing unused patches after each use.
- Use 1 patch for up to 12 hours.
Children 12 years or younger:
- Ask a doctor
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LENZAPRO FLEX
lidocaine/menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70512-013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 40 mg in 1 g LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength ACRYLIC ACID (UNII: J94PBK7X8S) Product Characteristics Color Score Shape RECTANGLE (White flexible patch) Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70512-013-15 3 in 1 BOX 02/01/2021 1 1 g in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/01/2021 Labeler - SOLA Pharmaceuticals (080121345)

