Cold Spot Point Relief by Fabrication Enterprises
Dosage form: ointment
Ingredients: MENTHOL 13mL in 90mL
Labeler: Fabrication Enterprises
NDC Code: 51452-002
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Active Ingredients: Menthol
Inactive Ingredients: deionized water, arnica, chondroitin sulfate, citirc acid, euclayptus oil, glucosamine sulfate, ilex paraguariesis leaf, isopropyl alcohol, peppermint oil, dimethyl sulfone, polysorbate-20, SD alcohol 40B.
Keep out of reach of children. If swallowed consult physician
Warnings Section: For external use only, avoid contact with eyes, do not apply to open wounds or damaged skin, if symptoms persist for more than seven days discontinue use and consult physician, keep out of reach of children and if swallowed consult physician, do not bandage tightly.
temporary relief of minor aches and pains of the muscles and joints
associated with simple backache, arthritis, bruises, strains and/or
|Labeler - Fabrication Enterprises (070577218)|
|Registrant - Fabrication Enterprises (070577218)|
Medically reviewed on Oct 5, 2018
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
More about Cold Spot Point Relief (menthol topical)
- Cold Spot Point Relief Side Effects
- During Pregnancy
- Dosage Information
- Drug class: topical rubefacient
- FDA Alerts (1)