OTC - ACTIVE INGREDIENT SECTION
Active ingredients:
Lidocaine HCL 4%
Menthol 4%
Active ingredients:
Lidocaine HCL 4%
Menthol 4%
Purpose:
Topical Anesthetic
Uses:
For the temporary relief of pain
Warnings:
For external use
Do 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 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 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 of skin injury, such as pain, swelling, or blistering where the product was applied.
If pregnant or breast-feeding, ask a health care professional before use.
Keep out of reach of children and pets.
If swallowed, get medical help or contact a Poison Control Center right away.
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 Information:
Avoid storing product in direct sunlight
Protect product from excessive mositure
Other Ingredients:
Acrylic Adhesive
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72189-148-15 | EA - Each | 72189-148 | ccebdf7f-4d27-4745-9266-9b9e1eaf2765 | 1 | 2021-05-05 |
| 70512-013-15 | EA - Each | 70512-013 | 2a3dd89e-8aed-4d3a-b817-bba1f2a0e083 | 1 | 2021-04-08 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72189-148 | 72189-148-15 |
| 70512-013 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| MAGNESIUM SULFATE, UNSPECIFIED | DE08037SAB | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| GLYCERYL 1-STEARATE | 258491E1RZ | IACT |
| POLYOXYL 100 STEARATE | YD01N1999R | IACT |
| DIMETHICONE 350 | 2Y53S6ATLU | IACT |
| TRIETHANOLAMINE LAURYL SULFATE | E8458C1KAA | IACT |
| ALOE | V5VD430YW9 | IACT |
| CETYL ALCOHOL | 936JST6JCN | IACT |
| MENTHOL, UNSPECIFIED FORM | L7T10EIP3A | ACTIB |
| LIDOCAINE | 98PI200987 | ACTIB |
| ALLANTOIN | 344S277G0Z | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| LenzaPro Flex | LIDOCAINE/MENTHOL | SOLA Pharmaceuticals | ba498f1d-460b-f4e6-e053-2995a90a5755 | 2025-12-08 | Warnings | 70512-013 |
| 0bc8f9ba-0cdb-a634-e063-6294a90aac0d | ea36a884-b247-4306-e053-2a95a90a8ebc | 2023-12-05 | Warnings | ea36a884-b247-4306-e053-2a95a90a8ebc |
Adverse event summaries are temporarily unavailable. Other product information remains available.