FDA.reportPublic FDA data

ECOLAB Burn Spray

Manufacturer
ECOLAB Food Safety Specialists, Inc.
Effective date
2024-01-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:14:49

Label at a glance#

ProductECOLAB Burn
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

Temporary pain relief associated with minor burns.

Dosage and administration

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

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Lidocaine HCl 2.0%

Purpose

OTC - PURPOSE SECTION

Topical pain relief

Uses

INDICATIONS & USAGE SECTION

Temporary pain relief associated with minor burns.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in large quantities, particularly over raw or blistered areas
  • near eyes, if this happens rinse thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 ingredients

INACTIVE INGREDIENT SECTION

decolorized aloe vera, germaben II, propylene glycol, purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-634-7680

Ecolab Burn Spray Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ECOLAB®

Burn Spray

Analgesic

Reorder # 43

Relieves pain in minor burns

Washable.

2 fl oz (59 mL)

Burn SprayBurn Spray

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71338-13871338-138-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
PROPYLPARABENZ8IX2SC1OHIACT
METHYLPARABENA2I8C7HI9TIACT

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
3e5d8d37-6d84-4af8-e063-6394a90af6684b6addc3-1615-1e33-e054-00144ff8d46c2025-09-09WarningsExact identifier
spl set id: 4b6addc3-1615-1e33-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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