FIRST AID BURN CREAM- first aid burn cream cream 
Front Line Safety

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Active Ingredient

Lidocaine Hydrochloride 0.5%

Purpose

Topical Analgestic

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Topical Antiseptic

Use(s)

• For the temporary relief of pain and itching associated with:

• Sunburn • Minor burns • Insect bites • Minor skin irritations • Cuts • Scrapes

Warnings

For External Use Only

Do not use

• In the eyes • Over large areas of the body or on deep puncture wounds, animal bites, or serious burns

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

Stop use and aks a doctor if

• The condition get worse • Condition clears up and recurs within a few days • Condition persists for more than 7 days

If pregnant or breast feeding

Ask a health care prfessional before use.

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 and over:

• Clean the affected area

• Apply a small amount of this product on the area 3 to 4 times daily

• May be covered with a sterile bandage

Children under 2 years: • Consult a doctor

Other Information

• Store in a cool, dry area 15º-25ºC (59º-77ºF)

• Tamper evident sealed packets

• Do not use any opened or torn packets

Inactive Ingredients

Butylated Hydroxytoluene, Cetomacrogol 1000, Cetostearyl Alcohol, Dimethicone, Glycerine, Glyceryl Monostearate, Isopropyl Myristate, Methylcellulose, Purified Water, Sodium EDTA, Sodium Methylparaben, Sodium Propylparaben

Questions?

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

Label

FL-2044_BX_MASTERFL-2044

FIRST AID BURN CREAM 
first aid burn cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58228-6244
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS50 mg  in 10000 mg
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 10000 mg
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)  
CETETH-20 (UNII: I835H2IHHX)  
METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
WATER (UNII: 059QF0KO0R)  
EDETATE SODIUM (UNII: MP1J8420LU)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
METHYLCELLULOSE (4000 MPA.S) (UNII: MRJ667KA5E)  
DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
Product Characteristics
Color    Score    
ShapeFREEFORMSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58228-6244-11800 in 1 CASE01/26/2024
125 in 1 BOX
1900 mg 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: 0f4ce2c2-f307-d95f-e063-6394a90ae7b3
Set id: 0f4ce2c2-f306-d95f-e063-6394a90ae7b3
Version: 1
Effective Time: 20240119
 
Front Line Safety