Medi-First Burn Spray

Manufacturer
Unifirst First Aid Corporation
Effective date
2025-09-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:13:00

Label at a glance#

ProductMedi-First Burn
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Lidocaine HCl 2.0%

OTC - PURPOSE SECTION

Purpose

Topical pain relief

INDICATIONS & USAGE SECTION

Uses

Temporary pain relief 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
  • near eyes, if this happens rinse thoroughly with water

OTC - STOP USE SECTION

Stop use and ask doctor if

condition worsens or persists for more than 7 days or clears up and returns.

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

  • spray an even layer of burn spray over cleaned affected area not more than 3-4 times daily
  • not to be used on children under 12 years of age

INACTIVE INGREDIENT SECTION

Inactive ingredients

glycerin, hydroxypropyl methylcellulose, melaleuca alterniflia (tea tree) leaf oil, octoxynol 9, PEG-40 hydronated castor oil, phenoxyethanol, propylene glycol, triethanolamine, water

OTC - QUESTIONS SECTION

Questions or comments? 1-800-634-7680

Medi-First Burn Spray Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Medi-First°

Burn Spray

Pump Spray

Lidocaine HCl 2.0%

Topical Analgesic

Relieves pain in minor burns

Store at 68°-77°F (20°-25°C)

2 FL OZ (59.1 ML)

MF BurnMF Burn

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1010769lidocaine HCl 2 % Topical SprayPSN5
1010769lidocaine hydrochloride 20 MG/ML Topical SpraySCD5
1010769lidocaine hydrochloride 2 % Topical SpraySY5

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-255-02Medi-First Burn0.0591 L in 1 BOTTLE, SPRAYSPRAY0.05915

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47682-25547682-255-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Medi-First BurnLIDOCAINE HCLUnifirst First Aid Corporationb3ebf104-cc51-0ef5-e053-2a95a90a25c92025-09-08WarningsExact identifier
ndc (package): 47682-255-02
ndc (product): 47682-255
ndc11 (package): 47682025502
spl id: 3e4cef3b-1395-fc54-e063-6294a90ad5f2
spl set id: b3ebf104-cc51-0ef5-e053-2a95a90a25c9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.