Green Guard Burn by Unifirst First Aid Corporation Green Guard Burn Spray

Green Guard Burn by

Drug Labeling and Warnings

Green Guard Burn by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GREEN GUARD BURN- lidocaine hcl spray 
Unifirst First Aid Corporation

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Green Guard Burn Spray

Drug Facts

Active ingredient

Lidocaine HCl 2.0%

Purpose

External analgesic

Uses

for the temporary relief of pain associated with minor burns

Warnings

For external use only.

Do not use in large quantities, particularly over raw or blisterd areas

When using this product avoid contact with eyes

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

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 3-4times daily
  • children under 2 years: consult a doctor

Other information

  • store at room temperature
  • you may report a serious adverse reaction to this product to 1-800-869-6970

Inactive ingredients

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

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 Spray

GREEN GUARD BURN 
lidocaine hcl spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 47682-320
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TEA TREE OIL (UNII: VIF565UC2G)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
OCTOXYNOL 9 (UNII: 7JPC6Y25QS)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 47682-320-020.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/202105/20/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01506/01/202105/20/2025
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 1/2024