Active Ingredient
Lidocaine HCL 4%
The following Structured Product Label (SPL) was submitted to the FDA by Prodigy Media Inc for the product Dr Lido (NDC 70171-0002). 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 active ingredient, purpose, uses, warnings, keep out of reach of children, direction, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine HCL 4%
External Analgesic
For the temporary relief of pain and itching associated with sunburns, minor cuts, insect bites, and skin irritations
Stop use and ask a doctor if
Do not use
If product is swallowed, get medical help or contact a Poison Control Center right away.
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: do not use, consult a physician.
Do not use if seal is broken.
Aqua (Deionized Water), Arnica Montana Flower Extract,C13-14 Isoparaffin, Chondroitin Sulfate, Dimethyl Sulfone (MSM), Emu Oil,
Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid,Tea Tree Oil, Triethanolamine.
Dr Lido label.jpg
Dr Lido Box.jpg
* Please review the disclaimer below.