Medi-First Burn Spray
- Manufacturer
- UniFirst First Aid Corporation
- Effective date
- 2024-01-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:14:03
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Lidocaine HCl 2.0%
OTC - PURPOSE SECTION
Purpose
External analgesic
INDICATIONS & USAGE SECTION
Uses
for the temporary relief of pain associated with minor burns
WARNINGS SECTION
Warnings
For external use only.
OTC - DO NOT USE SECTION
Do not use in large quantities, particularly over raw or blistered areas
OTC - WHEN USING SECTION
When using this product avoid contact with eyes
OTC - STOP USE SECTION
Stop use and ask a doctor if
- condition worsens
- symptoms persist for more than 7 days
- condition clears up and occurs again within a few days
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions
- adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily
- children under 2 years: consult a doctor
OTHER SAFETY INFORMATION
Other information
- store at room temperature
- you may report a serious adverse reaction to this product to 1-800-634-7680
INACTIVE INGREDIENT SECTION
Inactive ingredients
diazolidinyl urea, edetate disodium, glycerin, hypromellose, methylparaben, octoxynol 9, propylene glycol, propylparaben, tea tree oil, trolamine, water
OTC - QUESTIONS SECTION
Questions or comments? 1-800-634-7680
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Medi-First®
Burn Spray
Pump Spray
Lidocaine HCl 2.0%
Topical Analgesic
Relieves pain in monor burns
Store at room temperature
2 FL OZ (59.1 ML)
Products#
Every source-derived product name is available through these pages.
- Medi-First Burn
- Lidocaine HCl
- WATER
- LIDOCAINE HYDROCHLORIDE
- LIDOCAINE
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- OCTOXYNOL 9
- HYPROMELLOSE, UNSPECIFIED
- EDETATE DISODIUM
- METHYLPARABEN
- propylene glycol
- PROPYLPARABEN
- TEA TREE OIL
- TROLAMINE
- GLYCERIN
- DIAZOLIDINYL UREA
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 47682-250 | 47682-250-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| LIDOCAINE HYDROCHLORIDE | V13007Z41A | ACTIR |
| OCTOXYNOL 9 | 7JPC6Y25QS | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| propylene glycol | 6DC9Q167V3 | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| TEA TREE OIL | VIF565UC2G | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| DIAZOLIDINYL UREA | H5RIZ3MPW4 | IACT |
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 |
|---|---|---|---|---|---|---|
| 0f28beed-e8ad-0f29-e063-6294a90a8108 | bb7a14d8-b649-3052-e053-2a95a90a8fc7 | 2024-01-17 | Warnings | 0f28beed-e8ad-0f29-e063-6294a90a8108 bb7a14d8-b649-3052-e053-2a95a90a8fc7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
