Active Ingredient
Menthol 10.5 %
The following Structured Product Label (SPL) was submitted to the FDA by Sunflora Inc for the product Mineral Ice Methol Pain Relief (NDC 73240-905). 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, perpose, uses, directions, warning for external use only flammable, keep out of reach of children, inactive ingredeints, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Menthol 10.5 %
Topical Analgesic
Temporary relief from minor aches and pains of muscles and joints associated with
- simple backache
- strains, bruises, sprains
- provide cooling relief
Adultas and children 2 years of age and older, apply to affected area no more than 3 to 4 times daily. Children under
2 years of age: consult a doctor
When using this productAvoid sprying in eyes,
Do not use with heating pads or heating devices.
use only as directed, do notbandage tightly or use with heating pad, avoid contact with eyes and mucous membranes,
do notapply to wounds or damaged, brocken, or irritating skin, if severe burning sensation occurs, discontinue use immidiately.
Stop use and ask doctor ifcondition worsen, or symptoms persist for more than 7 days or clear up and occur again withing few days
Alcohol Denat
Arnica Montana Flower Extract
Calendula Officinalis Flower Extract
Camellia Sinensis Leaf Extarct
Chamomilla Recutita Flower Extract
Dimethyl Sulfone
Echinacea Angustifolia Extract
Ilex Paraguanensis Leaf Extarct
Isopropyl Myristate
Juniperus Communis Fruit Extract
Water
Whole Hemp Extarct
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