BURN EASE 3.5G- burn ease 3.5g gel 
Front Line Safety

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FL-3831

Active Ingredient

Lidocaine Hydrochloride 2%

Purpose

Analgesic

Use(s)

• For the temporary relief of pain associated with • Minor burns • Sunburn

Warnings

For External Use Only

Do not use

• On wounds or damaged skin

• In large quantities, particularly over raw surfaces or blistered areas

When using this product

• Avoid contact with the eyes • Do not bandage tightly

Stop use and ask a doctor if

• Condition worsens • Symptoms persist for more than 7 days • Symptoms clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily

Children under 2 year of age: Consult a doctor

Other Information

• Store at room temperature

Inactive Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Glycerin, Imidazolidinly Urea, Methylparaben, Propylene Glycol, Propylparaben, Purified Water, Tea Tree Leaf Oil, Triethanolamine

Questions?

1-888-900-2920 Monday - Friday 8AM-4PM PST

Label

FL-3831_BX_MASTERFL-3831

BURN EASE 3.5G 
burn ease 3.5g gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58228-6231
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
IMIDUREA (UNII: M629807ATL)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TEA TREE OIL (UNII: VIF565UC2G)  
Product Characteristics
Color    Score    
ShapeFREEFORMSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58228-6231-1480 in 1 CASE01/26/2024
120 in 1 BOX
13.5 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/26/2024
Labeler - Front Line Safety (061263699)

Revised: 1/2024
Document Id: 0f52021f-af8b-5b95-e063-6294a90a2c2a
Set id: 0f52021f-af8a-5b95-e063-6294a90a2c2a
Version: 1
Effective Time: 20240119
 
Front Line Safety