BURN N BITE- lidocaine, menthol gel 
Q.A. Laboratories

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.

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Burn N Bite

Drug Facts

Active Ingredient

Lidocaine 2%
Menthol 1%

Purpose

Ant-itch, Pain Relief

Uses

for the temporary relief of pain and discomfort caused by • minor burns • sunburn • scrapes • insect bites • minor skin irritations • rashes due to poison ivy, oak and sumac.

Warnings

For external use only.

When using this product

• Avoid contact with eyes

Do not use

• Under bandages or compresses

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or 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 right away.

Directions

Adults and children 2 years of age and older: Apply to the affected area not more than two times daily.

Children under 2 years of age: Do not use, consult a doctor

Inactive Ingredients

Deionized water, propylene glycol, aloe, isopropyl alcohol, carbomer, triethanolamine, phenoxyethanol

Questions or comments:

858-782-6627, 816-421-8081

Stanmar Laboratories     

Division of Q.A. Laboratories

404 Admiral Boulevard Kansas City, MO 64106

Ideazbrands.com

Made in the USA

Packaging

BURN N BITEBURN N BITE

BURN N BITE 
lidocaine, menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52099-9005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE2 g  in 100 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALOE (UNII: V5VD430YW9)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52099-9005-1141 g in 1 TUBE; Type 0: Not a Combination Product03/30/1994
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/30/1994
Labeler - Q.A. Laboratories (065361149)
Establishment
NameAddressID/FEIBusiness Operations
Q.A. Laboratories065361149manufacture(52099-9005)

Revised: 1/2022
Document Id: 4d0bfb71-7503-4386-9fb2-bf39d289a213
Set id: 283be206-8d1b-4508-a0a6-67200d78d46c
Version: 2
Effective Time: 20220117
 
Q.A. Laboratories