OTC - ACTIVE INGREDIENT SECTION
Active ingredient Purpose
Benzocaine USP 20%.......................................External analgesic
Benzalkonium Chloride 0.1%...........................First Aid Antiseptic
Active ingredient Purpose
Benzocaine USP 20%.......................................External analgesic
Benzalkonium Chloride 0.1%...........................First Aid Antiseptic
Uses
Temporarily relieves pain and itching due to: • sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritations• first aid to help prevent infection in minor cuts, scrapes, bites and burns
Warnings
For external use only.
Flammable: Do not use while smoking or near heat or flame Do not use in large quantities, particularly over raw surfaces or blistered areas
When using this product
• keep out of eyes
• do not apply over large areas of the body or in large quantites. in case of deep or puncture wounds, animal bites, or serious burns, concult a doctor
Stop use and ask doctor if
• condition gets worse • symptoms last more than 7 days
• symptoms clear up and occur again in a few days
•do not use longer than 1 week unless directed by doctor
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Directions • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor
Inactive Ingredients:
Alcohol Denat.
Diisopropyl Adipate
Propylene Glycol
Tocopheryl Acetate
| Class | Version | Type | Effective |
|---|---|---|---|
| BENZOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0363-7779-03 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-5146-f424-e053-dadaa90a57ce | Walgreens Drug Facts |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0363-7779-03 | Antiseptic Pain Relieving | 85 g in 1 CAN | SPRAY | 85 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0363-7779 | 0363-7779-03 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Benzalkonium Chloride | F5UM2KM3W7 | ACTIB |
| Benzocaine | U3RSY48JW5 | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| Diisopropyl Adipate | P7E6YFV72X | IACT |
| Propylene Glycol | 6DC9Q167V3 | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | 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 |
|---|---|---|---|---|---|---|
| f99f1d53-5eb8-4500-886d-7f3f6b127754 | 3c418897-e559-4bff-a1e4-ee1ca76269f8 | 2018-04-27 | Warnings | f99f1d53-5eb8-4500-886d-7f3f6b127754 3c418897-e559-4bff-a1e4-ee1ca76269f8 |
Adverse event summaries are temporarily unavailable. Other product information remains available.