FDA Label for Pain Relief
View Indications, Usage & Precautions
Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Pain Relieving Spray 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
USP Menthol 7%
Purpose
Topical Analgesic
Uses
Temporary relief of minor aches and pains of muscles and joints.
Warning
For external use only.
Flammable
Keep away from flame.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a poison control center right away. Avoid contact with eyes.
Otc - Do Not Use
Do not apply to open wounds or damaged skin. Do not bandage tightly.
Otc - Ask Doctor
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.
Directions
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.
Other Information
Store at room temperature.
Inactive Ingredients
Pain Relieving Spray, 4oz (118.3ml) . Topical Analgesic
Water, Isopropyl Alcohol, Glycerol, Eucalyptus Leaf Oil, Wintergreen Leaf Oil, Peppermint Oil, Coconut Oil.
Labeling
Pain Relieving Spray, 4fl.oz. (118.3mL0, Topical Analgesic
Menthol 7%,
Eucalyptus Oil, Glycerin, Isopropyl Alcohol, Wintergreen Oil, Purified Water, Tea Tree Oil
Pain Relieving Spray Inc., Bend, OR 97702-1971
* Please review the disclaimer below.
