OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Lidocaine ............. 0.5%
The DaVinci Company Lidocaine Ointment, USP 5%
- Manufacturer
- The Davinci Company | Inspec Solutions LLC.
- Effective date
- 2022-10-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:50:32
Label at a glance#
ProductThe Davinci Company
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure9 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Lidocaine 0.5% ............. Pain Reliever
INDICATIONS & USAGE SECTION
Temporary relief of pain and itching due to
- sunburn - minor burn - insect bites - minor cuts - scraps
WARNINGS SECTION
Warnings
For external use only
When using this product keep out of eyes
Rinse with warter to remove
OTC - STOP USE SECTION
Sop use and ask a doctor
system persist for more than 7 days.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If product is swallowed, get medical help or contact a poison control center right away.
DOSAGE & ADMINISTRATION SECTION
Direction
Adults and children 2 years and older: aooly to affected area not more that 3-4 times a day
Children under 2 years of age: consult a physician.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Aloe Barbadensis Leaf Extract, Carbomer, Diazolidinyl Urea, Disodium EDTA, Glycerin, Isopropyl Alcohol, Menthol, Polysorbate 80, Propylene Glycol, Triethanolamine, Water, Yellow 5.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 82951-001-01 | 2025-12-15 | C162847 | 48780-1 | 1030e365-4a85-111a-e063-dadaa90a10e2 | The DaVinci Company Lidocaine Ointment, USP 5% |
| 82951-001-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4a85-111a-e063-dadaa90a10e2 | The DaVinci Company Lidocaine Ointment, USP 5% |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- The Davinci Company
- Lidocaine
- WATER
- ALOE VERA LEAF
- ASCORBIC ACID
- LYSINE HYDROCHLORIDE
- TRICAPRYLIN
- CHOLECALCIFEROL
- SUNFLOWER OIL
- CHAMOMILE FLOWER OIL
- PUNICA GRANATUM ROOT BARK
- SILICON DIOXIDE
- SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA
- TRIETHOXYCAPRYLYLSILANE
- ZINC OXIDE
- MINERAL OIL
- OCTYLDODECANOL
- ETHYLHEXYLGLYCERIN
- HYDROCORTISONE
- PYRIDOXINE HYDROCHLORIDE
- STEARIC ACID
- .ALPHA.-TOCOPHEROL ACETATE
- PEG-8 DIMETHICONE
- PETROLATUM
- PHENOXYETHANOL
- PROPYLENE GLYCOL
- HYALURONATE SODIUM
- LIDOCAINE HYDROCHLORIDE
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82951-001 | 82951-001-01 |
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 |
|---|---|---|---|---|---|---|
| 45fe79a8-3d5b-9f4e-e063-6294a90a8cf5 | ebf19dc9-c930-340c-e053-2a95a90adb7f | 2025-12-15 | Warnings | ebf19dc9-c930-340c-e053-2a95a90adb7f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.