FDA Label for Menthol
View Indications, Usage & Precautions
Menthol Product Label
The following document was submitted to the FDA by the labeler of this product Jag Alliance, Llc. 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 Ingredient
Menthol 10%
Purpose
Topical Analgesic
Uses
Aid for temporary local relief of minor pain in muscles or joints.
Warnings
- For external use only.
- Avoid contact with eyes.
- If symptoms persist for more than seven days, discontinue use and consult a physician.
- Ask a health professional before use.
IF PREGNANT OR BREAST – FEEDING:
Keep Out Of Reach Of Childen:
- If swallowed, get medical help or contact a Poison Control Center right away.
- Emergency Number: 1-800-222-1222
Directions:
Adults and children two-years of age or older:
- Apply to affected area not more than three to four times daily.
- Children under two-years of age: consult a physician.
Additional Information
Store at room temperature.
Inactive Ingredients
Aqua, Caprylic/Capric Triglyceride, Alcohol Denat., Stearic Acid, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol, Helianthus Annuus Seed Oil, Butyrospermum Parkii Butter, Cannabis Sativa Seed Oil, Glycereth-26, Persea Gratissima Oil, Stearyl Alcohol, Sodium Polyacrylate, Aloe Barbadensis Leaf Extract, Glycerin, Boswellia Serrata Extract, Melaleuca Alternifolia Leaf Oil, Mentha Arvensis Herb Oil, Arnica Montana Flower Extract.
* Please review the disclaimer below.