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Burn Relief Leader

Medically reviewed on January 11, 2018

Dosage form: spray
Ingredients: Lidocaine .05g in 100g
Labeler: Cardinal Health
NDC Code: 37205-613

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Lidocaine 0.50%

Uses

Temporarily relieves pain and itching due to:  sunburn, minor burns, minor cuts, scrapes, insect bites, minor skin irritations.

Warnings

For external use only.  Flammable:  do not use while smoking or near heat or flame.  Do not use in large quantities, particularly over raw surfaces or blistered areas.  When using this product:  keep out of eyes, use only as directed, do not puncture or incinerate.  Contents under pressure.  Do no store at temperatures above 120 deg F. Stop use and ask doctor if:  condition gets worse, symptoms last more than 7 days, or symptoms clear up and occur again in a few days. 

Directions

Shake well.  Adults and children 2 years of age and older:  apply to affected area not more than 3 to 4 times daily.  Children under 2 years of age:  ask a doctor.  To apply to face, spray into palm of hand and gently apply.

Inactive ingredients

Aloe Barbadensis Leaf Juice, SD Alcohol 40, Propylene Glycol, Glycerin, Simethicone, Tocopheryl Acetate, Triethanolamine, Carbomer, Diazolidinyl Urea, Methylparaben, Propylparaben, Disodium Cocoamphodipropionate, Disodium EDTA.

Purpose

External analgesic.

Keep out of reach of children.

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

Burn Relief Spray with Lidocaine.


BURN RELIEF  LEADER
lidocaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37205-613
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lidocaine (Lidocaine) Lidocaine.05 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Aloe 
Alcohol 
Propylene Glycol 
Glycerin 
.ALPHA.-TOCOPHEROL ACETATE, D- 
CARBOMER HOMOPOLYMER TYPE C 
DIAZOLIDINYL UREA 
Methylparaben 
Propylparaben 
Edetate Disodium 
Packaging
#Item CodePackage Description
1NDC:37205-613-11127 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34812/01/2011
Labeler - Cardinal Health (097537435)

 
Cardinal Health

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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