Burn N Bite
FDA Label NDC 52099-9005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Q.a. Laboratories for the product Burn N Bite (NDC 52099-9005). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredient, purpose, uses, warnings, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 Bite (Label)
Burn N Bite (Label)
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