Active Ingredients
Camphor 3.00%
Menthol 2.00%
Neuroflex Topical Pain Relieving Liquid Solution
FDA Label NDC 69876-1740
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Almark Products Inc for the product Neuroflex Topical Pain Relieving Liquid (NDC 69876-1740). 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 ingredients, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Pain Reliever
Uses
For temporary relief of minor aches and pains of muscles and joints:
• arthritis • simple backaches • soreness • strains • sprains • bruises
Warnings
For External Use Only
Flammable: Keep away from fire or flame.
Do Not Use
• on wounds • on damaged skin • on mucous membranes
When Using This Product
• avoid contact with eyes • do not bandage tightly • do not use a heating pad
Stop Use And Ask A Doctor If
• condition worsens • symptoms persist for more than 7 days • symptoms 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 affected areas not more than 3 to 4 times daily. No need to rub in.
• Children under 2 years of age: Consult a physician.
Inactive Ingredients
Eucalyptus Globulus Lead (Eucaluptus) Oil, Melaleuca, Alternifolia (australian Tea Tree) Leaf Oil, Pinus Sylvestris (Pine) Oil, Polysorbate-20, SD-Alcohol 40B.
Package Labeling:
Label (Label)
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