5Kind Neurophase Pro Pain Relieving
- Product NDC
- 85978-016
- 11-digit product format
- 859780016
- Labeler code
- 85978
- Product ID
- 85978-016_5b872e88-3a84-01e2-e063-6394a90a774b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE, MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- 5KIND TRADING LTD
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-04
- 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
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 5Kind Neurophase Pro Pain Relieving
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| LIDOCAINE HYDROCHLORIDE | 40 mg/mL |
| MENTHOL | 10 mg/mL |
openFDA label cross-check#
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 85978-016-00 | 85978001600 | 118 mL in 1 JAR (85978-016-00) | 118 ml | 2026-09-04 | No | No | Current |