Green Guard Burn Spray

Manufacturer
Unifirst First Aid Corporation
Effective date
2024-01-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:14:03

Label at a glance#

ProductGreen Guard Burn
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure13 sections

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 blisterd 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 3-4times 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 1-800-869-6970

INACTIVE INGREDIENT SECTION

Inactive ingredients

diazolidinyl urea, edetate disodium, glycerin, hypromellose, methylparaben, octoxynol 9, propylene glycol, propylparaben, tea tree oil, trolamine, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Burn Spray

Lidocaine HCl 2.0%

Topical Pain Relief

Rekieves pain of minor burns

Store at room temperature

Green Guard®

2 fl oz (59.1 mL)

Burn SprayBurn Spray

Products#

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DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47682-32047682-320-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
0f2726f1-56fd-0083-e063-6294a90a506abc80a337-31ea-85f6-e053-2995a90a26632024-01-17WarningsExact identifier
spl id: 0f2726f1-56fd-0083-e063-6294a90a506a
spl set id: bc80a337-31ea-85f6-e053-2995a90a2663

Reported adverse events (FAERS/openFDA)#

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