Otc - Active Ingredient
Active ingredient
Lidocaine HCI 2%
Lightning Products Burn Relief Spray
FDA Label NDC 43473-070
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nantong Health & Beyond Hygienic Products Inc. for the product Lightning Products Burn Relief (NDC 43473-070). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
External Analgesic
Indications & Usage
Uses
For temporary relief of pain associated with minor burns.
Warnings
Warnings
For external use only.
Avoid contact with eyes
Otc - Do Not Use
Do not use
■ in large quantities, particularly over raw surface or blistered areas
Otc - Stop Use
Stop use and ask a doctor
- if the condition worsens
- symptoms persist for more than 7 days
- condition clears up and occurs again within a few days
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Dosage & Administration
Directions
Adults and children 2 years of age or older:apply to affected area not more than 3 to 4 times daily
Chilrdren under 2 years old: consult a doctor
Inactive Ingredient
Inactive ingredients
glycerin, Hydroxypropyl methylcellulose, melaleuca alterniflia (tea tree) leaf oil, octoxyol 9, PEG-40 hydrogenated castor oil, Phenoxyethanol, Polyethylene Glycol, Aminomethyl Propanol, Water
* Please review the disclaimer below.
