Launch Medical Cream
FDA Label NDC 54723-018
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sambria Pharmaceuticals, Llc for the product Launch Medical (NDC 54723-018). 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, directions, inactive ingredients, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Lidocaine HCL 4.0% w/w
Purpose
External Analgesic
Uses
For temporary relief of pain and itching.
Warnings
- For external use only.
- Avoid contact with eyes.
- Do not use in large quantities, particularly over raw surfaces or blistered areas.
- If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with a few days, discontinue use of this product and consult a doctor.
- If product is swallowed get medical help or contact a Poison Control Center right away.
Directions
- Apply in a circular motion for 30 to 60 seconds over intact skin.
- For adults and children two-years and older, apply to affected area not more than 3 to 4 times daily.
- Children under 2 years of age consult a physician.
Inactive Ingredients
Arnica Montana Flower Extract, C13-14 Isoparaffin, Dimethyl Sulfone (MSM), Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Sodium Chondroitin Sulfate, Stearic Acid, Triethanolamine, Water
Other Information
Protect this product from excessive heat and direct sun.
Questions?
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Product Label
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