Indications and uses
For temporary relief of pain
Lidozen Patch
- Manufacturer
- Village Pharma, LLC
- Effective date
- 2023-11-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 00:02:56
Label at a glance#
ProductLidozen
Active ingredientLIDOCAINE, MENTHOL
Label structure7 sections
Dosage and administration
Clean and dry affected area. Remove patch from backing and apply to affected area. Use only one patch at a time, and maximum of four patches / day. Leave patch on affected area for up to 8 hours Do not use patches for longer than five consecutive days, Children under 12 should consult physician prior to use.
Label contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Lidocaine 4.00%
Menthol 1.00%
OTC - PURPOSE SECTION
Topical Anesthetic
External Analgesic
USES:
For temporary relief of pain
WARNINGS:
- For external use only.
- Avoid contact with eyes.
- If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.
Do not use
- in large quantities, particularly over raw surfaces or blistered areas.
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
- If swallowed, get medical help or contact a Poison Control Center right away.
DIRECTIONS (Adults and Children Over 12 Years):
Clean and dry affected area.
Remove patch from backing and apply to affected area.
Use only one patch at a time, and maximum of four patches / day.
Leave patch on affected area for up to 8 hours
Do not use patches for longer than five consecutive days,
Children under 12 should consult physician prior to use.
INACTIVE INGREDIENTS:
Water, Glycerol, Sodium Polyacrylate, Propylene Glycol, Polysorbate 80, Tartaric Acid, Dihydroxyaluminium Aminoacetate, Methylparaben
SPL UNCLASSIFIED SECTION
Store below 25 degrees Celsius, Avoid directe sunlight.
Package Labeling:
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1249758 | lidocaine 4 % / menthol 1 % Medicated Patch | PSN | 3 |
| 2201504 | Lidozen 4 % / 1 % Medicated Patch | PSN | 3 |
| 2201504 | lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch [Lidozen] | SBD | 3 |
| 1249758 | lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch | SCD | 3 |
| 1249758 | lidocaine 4 % / menthol 1 % Medicated Patch | SY | 3 |
| 2201504 | Lidozen (lidocaine 4 % / menthol 1 % ) Medicated Patch | SY | 3 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| LIDOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71574-900-05 | Lidozen | 5 in 1 POUCH | PATCH | 5 | 3 | |
| 71574-900-05 | Lidozen | 1 g in 1 PATCH | PATCH | 1 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71574-900-05 | EA - Each | 71574-900 | fc64d060-4f39-43bd-b8fe-ff30f63419e1 | 1 | 2020-03-10 |
Products#
Every source-derived product name is available through these pages.
- Lidozen
- LIDOCAINE, MENTHOL
- WATER
- GLYCERIN
- PROPYLENE GLYCOL
- POLYSORBATE 80
- TARTARIC ACID
- DIHYDROXYALUMINUM AMINOACETATE
- METHYLPARABEN
- LIDOCAINE
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71574-900 | 71574-900-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| TARTARIC ACID | W4888I119H | IACT |
| DIHYDROXYALUMINUM AMINOACETATE | DO250MG0W6 | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| LIDOCAINE | 98PI200987 | ACTIB |
| MENTHOL | L7T10EIP3A | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 0b581dc2-c9a7-4792-e063-6394a90a7db3 | 00171d6f-a0a7-4e90-abde-6dd3f1285ec0 | 2023-11-29 | Warnings | 0b581dc2-c9a7-4792-e063-6394a90a7db3 00171d6f-a0a7-4e90-abde-6dd3f1285ec0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.