OTC - ACTIVE INGREDIENT SECTION
Lidocaine 5%
Lidocaine 5%
Topical anesthetic
For temporary relief of local discomfort, itching, pain, soreness.
For external use only. Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days, or clear up and occur again within a few days. When using this product avoid contact with eyes. Flush with water if contact occurs. Do not apply over large areas of the body, particularly over raw surfaces or blistered areas.
Pregnant or breastfeeding, ask a health professional before use.
Aloe barbadebsis leaf juice (Aloe vera), Water, Lecithin (Soybean), PropyleneGlycol, Tocopheryl Acetate, Carbomer, Menthol, Triethanolamine.
If swallowed, get medical help or contact a Poison Control Center right away.
• When practical, clean area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet
tissue or soft cloth before applying.
• Adults and children 12 years and older: apply externally to the affected area up to 6 times a day.
• Children under 12 years of age: consult a doctor.
Adults and children 12 years and older: For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product.
Apply externally up to 6 times per day.
Children under 12: Consult a Doctor.
Keep away from direct sunlight or heat
Store in room temperature (59-86°F/15-30°C)
NDC: 82929-012-08 10ml in 1 Tube
NDC: 82929-012-09 40ml in 1 Tube
NDC: 82929-012-10 60ml in 1 Tube
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 82929-012 | 82929-012-08, 82929-012-09, 82929-012-10 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| LECITHIN, SOYBEAN | 1DI56QDM62 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| LIDOCAINE | 98PI200987 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| MENTHOL | L7T10EIP3A | IACT |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
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 |
|---|---|---|---|---|---|---|
| e607c219-94da-503b-e053-2a95a90aad27 | e607c219-94d9-503b-e053-2a95a90aad27 | 2022-08-12 | Warnings | e607c219-94da-503b-e053-2a95a90aad27 e607c219-94d9-503b-e053-2a95a90aad27 |
Adverse event summaries are temporarily unavailable. Other product information remains available.