Active Ingredient
Menthol 8.0%
The following Structured Product Label (SPL) was submitted to the FDA by Medline Industries, Lp for the product Activice (NDC 53329-984). 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, uses, warnings, when using this product, stop use and ask doctor if, if pregnant or breastfeeding,, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Menthol 8.0%
Topical Analgesic
For the temporary relief of minor aches and pains of muscles and joints associated with:
For external use only.
Avoid contact with eyes.
Flammable: keep away from fire or flame.
When using this product
ask a health professional before use.
If swallowed, get medical helop or contact a Poison Control Center right away.
Adults and children over 12 years:
apply directly onto affected area without the need to bandage
repeat if necessary, but do not apply more than 4 times daily.
Children 12 years or younger: ask a doctor.
acrylic acid/vinyl ester copolymer, dimethylsulfone (MSM),
eucalyptus oil, glucosamine sulfate, hydroxypropylcellulose, SD alcohol 39C, PEG-8 dimethicone,
pentylene glycol, peppermint oil, triethanolamine, water (USP).
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