LidoPro
- Product NDC
- 83881-403
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- lidocaine and menthol
- Dosage form
- PATCH
- Route
- TRANSDERMAL
- Labeler
- Clinic Pharma
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Substance
- LIDOCAINE; MENTHOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 83881-403-01 | 1 PATCH in 1 POUCH (83881-403-01) / 10 g in 1 PATCH | 2026-03-11 | | No | Historical |
| 83881-403-15 | 15 POUCH in 1 CARTON (83881-403-15) / 1 PATCH in 1 POUCH / 10 g in 1 PATCH | 2026-03-11 | | No | Historical |
| 83881-403-30 | 30 POUCH in 1 CARTON (83881-403-30) / 1 PATCH in 1 POUCH / 10 g in 1 PATCH | 2026-03-11 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LidoPro Patch | Advanced Rx of Tennessee, LLC | 2026-04-17 | HUMAN OTC DRUG LABEL | 1 |
| LidoPro Patch | Clinic Pharma | 2026-03-25 | HUMAN OTC DRUG LABEL | 1 |