Otc - Active Ingredient
Menthol 1.00%
The following Structured Product Label (SPL) was submitted to the FDA by Easment Llc for the product Easment Dmso Cream (NDC 87352-002). 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 otc - active ingredient, otc - purpose, dosage & administration, warnings, otc - do not use, otc - when using, otc - ask doctor, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Menthol 1.00%
Topical Analgesic
For the temporary relief of minor aches and pains of muscles and joints.
For external use only.
If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.
WATER, DIMETHYL SULFOXIDE, ALOE BARBADENSIS LEAF JUICE, CAPRYLIC/CAPRICTRI GLYCERIDE, CETEARYL ALCOHOL DIMETHYL SULFONE, GLYCERIN, GLYCERYLSTEARATE, PEG-100 STEARATE, SODIUM ACRYLATES COPOLYMER, ARNICA MONTANA FLOWER EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, BUTYROSPERMUMPARKII (SHEA) BUTTER, MAGNESIUM CHLORIDE, METHYLENE BIS-BENZOTRIAZOLYLTETRAMETHYLBUTYLPHENOL LECITHIN, DIMETHICONE, TOCOPHERYL ACETATE,CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, CARBOMER, LAVANDULAANGUSTIFOLIA(LAVENDER) OIL CURCUMALONGA(TURMERIC) ROOT EXTRACT, DECYL GLUCOSIDE,ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, CAPSAICIN, AMINOMETHYLPROPANOL, SODIUM CITRATE, MENTHYL LACTATE, SORBITOL, ACRYLATES COPOLYMER
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