Active Ingredient
Menthol 1.5%
Celadrin
FDA Label NDC 31586-2683
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Natural Factors Nutritional Products Ltd for the product Celadrin (NDC 31586-2683). 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 ingredient, purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Pain relieving cream
Use
Temporarily relieves minor aches and pains of musclesand joints associated with:simple backachearthritisstrainsbruisessprains
Warnings
For external use only
Do Not Use
On wounds or damaged skin
When Using This Product
- avoid contact with eyes or mucous membranes
- do not bandage tightly
Stop Use And Ask A Doctor If
- condition worsens or symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
Directions
- Adult and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
- Children under 2 years of age: consult a physician.
Inactive Ingredients
Aloe vera gel, celadrin® proprietary blend of esterified fatty acids (7.5%), cetyl alcohol, cinnamon oil, eucalyptus oil, glyceryl stearate, grape seed oil, hypromellose, jojoba oil, peppermint oil, potassium sorbate, purified water, squalane, stearic acid, stearyl alcohol, tea tree oil, vegetable glycerin, wintergreen oil.
Package Label.Principal Display Panel
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