LenzaPro Flex
- Product NDC
- 70512-013
- 11-digit product format
- 705120013
- Labeler code
- 70512
- Product ID
- 70512-013_457278e8-31e5-637e-e063-6394a90a808d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine/Menthol
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- SOLA Pharmaceuticals
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-02-01
- Substance
- LIDOCAINE; MENTHOL
- Active strength
- 40; 40 mg/g; mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LenzaPro Flex
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE | 40 mg/g |
| MENTHOL | 40 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 98PI200987, L7T10EIP3A |
| Rxcui | 2572014 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70512-013-15 | LenzaPro Flex | 3 in 1 BOX | PATCH | 3 | | 7 |
| 70512-013-15 | LenzaPro Flex | 1 g in 1 POUCH | PATCH | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70512-013 | LENZAPRO FLEX (LIDOCAINE/MENTHOL) PATCH [SOLA PHARMACEUTICALS] | 6 | Current NDC, Legacy NDC, 2 package rows | 20240522_ba498f1d-460b-f4e6-e053-2995a90a5755.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70512-013-15 | 70512001315 | 3 POUCH in 1 BOX (70512-013-15) / 1 g in 1 POUCH | 3 pouch | 2021-02-01 | 0000-00-00 | No | No | Current |