BURN N BITE- lidocaine, menthol gel

BURN N BITE by

Drug Labeling and Warnings

BURN N BITE by is a Otc medication manufactured, distributed, or labeled by Q.A. Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

BURN N BITE 
lidocaine, menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52099-9005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	2 g  in 100 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE (UNII: V5VD430YW9)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52099-9005-1	141 g in 1 TUBE; Type 0: Not a Combination Product	03/30/1994

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/30/1994

Labeler - Q.A. Laboratories (065361149)

Establishment
Name	Address	ID/FEI	Business Operations
Q.A. Laboratories		065361149	manufacture(52099-9005)