Active Ingredients
USP Menthol 7%
The following Structured Product Label (SPL) was submitted to the FDA by Pain Relieving Spray Inc. for the product Pain Relief (NDC 84638-8201). 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, warning, keep out of reach of children., otc - do not use, otc - ask doctor, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
USP Menthol 7%
Topical Analgesic
Temporary relief of minor aches and pains of muscles and joints.
For external use only.
Flammable
Keep away from flame.
If swallowed get medical help or contact a poison control center right away. Avoid contact with eyes.
Do not apply to open wounds or damaged skin. Do not bandage tightly.
Consult a doctor if excessive skin irritation occurs, or if you are prone to allergic reactions to salicylates,including aspirin. If condition worsens, if symptoms persist for more than 7 days or clear up and recur again within a few days, discontinue use of this product and consult a doctor.
For adults and children 2 years of age and older: Shake well and apply to affected area not more than 3-4 times daily. Will not stain clothing. For children under 2 years of age, consult a doctor.
Store at room temperature.
Pain Relieving Spray, 4oz (118.3ml) . Topical Analgesic
Water, Isopropyl Alcohol, Glycerol, Eucalyptus Leaf Oil, Wintergreen Leaf Oil, Peppermint Oil, Coconut Oil.
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