Dosage and administration
Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. Children under two-years of age consult a physician.
Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. Children under two-years of age consult a physician.
Menthol 1.25%
Topical Pain Relief
For the temporary relief of minor aches and pains of the muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.
If swallowed, consult physician.
contact physician prior to use.
Achillea millefolium (yarrow) extract, Aloe barbadensis (aloe vera gel) juice, aqua (deionized water), Arnica montana (arnica) extract, beeswax, Bixa orellana (annatto) seed extract, Boswellia serrata extract, Calendula officinalis (marigold) flower extract, caprylic/capric triglyceride, cetearyl olivate, cetyl myristoleate, curcuma longa (turmeric) extract, dimethyl sulfone (msm), emu oil, gluconolactone, glycerin, glyceryl stearate se, Harpagophytum procumbens (devils claw) root extract, Helianthus annuus (sunflower) seed oil, Ilex paraguariensis (yerba mate) leaf extract, magnesium sulfate, Mentha piperita (peppermint) oil, Scutellaria baicalensis (baikal skullcap) root extract, sodium benzoate, sorbitan olivate, stearic acid, tocopheryl acetate (vitamin e), xanthan gum, yucca extract.
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 69896-728 | 69896-728-01 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 0723fe60-78ea-b7c4-e063-6294a90added | ef3eead6-bf7a-4a76-bfee-2a5d5c92946c | 2023-10-07 | Warnings | ef3eead6-bf7a-4a76-bfee-2a5d5c92946c |
Adverse event summaries are temporarily unavailable. Other product information remains available.