Lidochill(TM) Gel
- Product NDC
- 59088-240
- 11-digit product format
- 590880240
- Labeler code
- 59088
- Product ID
- 59088-240_3e4f5664-2734-582d-e063-6294a90a41ed
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl 4%, Menthol 1%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-08
- Substance
- LIDOCAINE HYDROCHLORIDE; MENTHOL
- Active strength
- 40; 10 mg/mL; mg/mL
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| V13007Z41A | LIDOCAINE HYDROCHLORIDE | 6108-05-0 | LIDOCAINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-240-16 | 59088024016 | 237 mL in 1 BOTTLE, PUMP (59088-240-16) | 237 ml | 2025-09-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lidochill(TM) Gel | PureTek Corporation | 2025-09-08 | HUMAN OTC DRUG LABEL | 5 |