FDA Label for Neuroflex Topical Pain Relieving Liquid
View Indications, Usage & Precautions
Neuroflex Topical Pain Relieving Liquid Product Label
The following document was submitted to the FDA by the labeler of this product Almark Products Inc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredients
Camphor 3.00%
Menthol 2.00%
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:
* Please review the disclaimer below.