Indications and uses
For Temporary relief of pain
Lidozen Patch
- Manufacturer
- Village Pharma, LLC
- Effective date
- 2023-01-24
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:39:03
Label at a glance#
ProductLidozen
Active ingredientLIDOCAINE HYDROCHLORIDE, 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 HCL 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:
Aloe Barbadensis Leaf (Aloe Vera Juice) Gel, Aqua (Deionized Water), Arnica Montana Extract, Boswellia Serrata Extract, Camellia Sinensis Leaf (Green Tea) Extract, Carbomer, Ethylhexylglycerin, Glycerin, Isopropyl Myristate, PEG-8, Phenoxyethanol, Polysorbte-80, Sodium Lauryl Sulfate, Triethanolamine, FD&C Blue #1, FD&C Yellow #5
SPL UNCLASSIFIED SECTION
Store below 25 degrees Celsius. Avoid direct sunlight.
Package Labeling:
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71574-400-05 | EA - Each | 71574-400 | 3645d39e-0755-4fb6-90ea-a584b98d430e | 1 | 2017-10-13 |
Products#
Every source-derived product name is available through these pages.
- Lidozen
- LIDOCAINE HYDROCHLORIDE, MENTHOL
- ALOE VERA LEAF
- WATER
- ARNICA MONTANA
- INDIAN FRANKINCENSE
- GREEN TEA LEAF
- CARBOXYPOLYMETHYLENE
- ETHYLHEXYLGLYCERIN
- GLYCERIN
- ISOPROPYL MYRISTATE
- POLYETHYLENE GLYCOL 400
- PHENOXYETHANOL
- POLYSORBATE 80
- SODIUM LAURYL SULFATE
- TROLAMINE
- FD&C BLUE NO. 1
- FD&C YELLOW NO. 5
- LIDOCAINE HYDROCHLORIDE
- LIDOCAINE
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71574-400 | 71574-400-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 071d124a-b535-339f-e063-6294a90a101c | 55c53f81-9418-33e1-e054-00144ff8d46c | 2023-10-07 | Warnings | 55c53f81-9418-33e1-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.