LenzaPro Flex Path
- Product NDC
- 72189-361
- 11-digit product format
- 721890361
- Labeler code
- 72189
- Product ID
- 72189-361_e2aab4b8-d94d-a38a-e053-2a95a90a2795
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LenzaPro Flex Path
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Direct_Rx
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-06-22
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE; MENTHOL
- Active strength
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-361-15 | 72189036115 | 3 g in 1 BOX (72189-361-15) | 3 g | 2022-06-22 | 0000-00-00 | No | No | Current |