OTC - ACTIVE INGREDIENT SECTION
Benzocaine 20%, Menthol 0.5%
Benzocaine 20%, Menthol 0.5%
Topical Analgesic
For the temporary relief of pain and itching associated with sunburn, minor skin irritations, insect bites, scrapes, minor cuts, and minor burns.
For external use only. Flammable--Keep away from fire or flame. Allergyalert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics. When using this product avoid contact with eyes. Do not spray in the face or mouth. Use only as directed. Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days, itching, rash or irritation develops.
If swallowed, get medical help or contact a Poison Control Center right away.
Adults and children 2 years of age and older, apply to the affected area not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor. To use this product, hold the can 6 to 12 inches away from the affected area. Direct spray nozzle towards skin and press the button to activate the spray. To apply to face, spray into palm of hand and gently apply.
Acetylated Lanolin Alcohol, Alcohol Denat., Aloe Barbadensis Leaf Extract, Cetyl Acetate, Helianthus Annuus (Sunflower) Seed Oil, PEG-8 Laurate, Polysorbate 85.
| Class | Version | Type | Effective |
|---|---|---|---|
| BENZOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72839-343-03 | Pain, Burn, and Itch Relief | 85 g in 1 CAN | SPRAY | 85 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72839-343 | 72839-343-03 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETYLATED LANOLIN ALCOHOLS | SNN716810P | IACT |
| BENZOCAINE | U3RSY48JW5 | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| CETYL ACETATE | 4Q43814HXS | IACT |
| SUNFLOWER OIL | 3W1JG795YI | IACT |
| PEG-8 LAURATE | 762O8IWA10 | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| POLYSORBATE 85 | A7F3N56197 | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | 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 |
|---|---|---|---|---|---|---|
| Pain, Burn, and Itch Relief | BENZOCAINE 20%, MENTHOL 0.5% | Derma Care Research Labs, LLC | fd9fe09f-3ae9-c5f5-e053-6394a90ad691 | 2024-12-19 | Warnings | 72839-343-03 72839-343 72839034303 29a5d04c-286a-9659-e063-6294a90a30bc fd9fe09f-3ae9-c5f5-e053-6394a90ad691 |
Adverse event summaries are temporarily unavailable. Other product information remains available.