Otc - Active Ingredient
Lidocaine 4%
The following Structured Product Label (SPL) was submitted to the FDA by Sola Pharmaceuticals for the product Lidaflex (NDC 70512-012). 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 - when using, otc - stop use, otc - pregnancy or breast feeding, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine 4%
Topical Anesthetic
For temporary relief of pain
For external use only
Do not use
When using this product
Stop use and ask a doctor if
If Pregnant or breast-feeding
Ask a health professional before use.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Adults and Children 12 years of age and over:
Children under 12 years of age: Consult a doctor
Acrylic Adhesive, Flaxseed oil, and Polysorbate 80
Manufactured for:
SOLA Pharmaceuticals
655 Highlandia Dr. Ste B
Baton Rouge, LA 70810
Avoid storing product in direct sunlight
Protect product from excessive moisture
For questions for comments call 866-747-7365
LidaFlex Patch
Topical Pain Patch
For temporay pain relief
NDC 70512-012-30
Qty: 30 Flex Patches
(5 per Resealable Pouch) x 6
* Please review the disclaimer below.