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.
MINTED LEAF Cold Therapy Foot Relief with CBD + Menthol Gel
- Manufacturer
- MMG Consumer Brands, LLC
- Effective date
- 2024-12-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:46:43
Label at a glance#
ProductMINTED LEAF Cold Therapy Foot Relief with CBD and Menthol
Active ingredientMENTHOL
Label structure7 sections
Label contents#
Full prescribing information#
Active ingredient
Menthol 16.00%
Purpose
Topical Analgesic
Indications
- For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis
- simple backache
- sprains
- bruises and strains.
Warnings:
- For external use only.
- Avoid contact with eyes.
- If symptoms persist for more than seven days, discontinue use and consult physician.
Keep out of reach of children.
If swallowed, consult physician.
Do not apply
- to wounds or damaged skin.
- Do not bandage tightly.
If pregnant or breast feeding,
contact physician prior to use.
Directions
- 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.
Additional Information
- Store at room temperature.
Other Ingredients:
Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Extract, Betaglucan, Cannabis Sativa (Full Spectrum Hemp) Oil, Caprylic/Capric Triglyceride, Cetearyl Olivate, Gluconolactone, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Petrolatum, Sodium Benzoate, Sodium Polyacrylate, Sorbitan Olivate, Stearic Acid, Tocopheryl Acetate (Vitamin E), Urea, Xanthan Gum, Zemea (Corn) Propanediol.
Package Labeling:
Products#
Every source-derived product name is available through these pages.
- MINTED LEAF Cold Therapy Foot Relief with CBD and Menthol
- MENTHOL
- ALOE VERA LEAF
- WATER
- ARNICA MONTANA
- CANNABIS SATIVA WHOLE
- MEDIUM-CHAIN TRIGLYCERIDES
- CETEARYL OLIVATE
- GLUCONOLACTONE
- GLYCERIN
- GLYCERYL MONOSTEARATE
- SUNFLOWER OIL
- ISOPROPYL ALCOHOL
- DIMETHYL SULFONE
- PETROLATUM
- SODIUM BENZOATE
- SORBITAN OLIVATE
- STEARIC ACID
- .ALPHA.-TOCOPHEROL ACETATE
- UREA
- XANTHAN GUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73102-064 | 73102-064-00 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| 2922258b-c665-13d3-e063-6394a90abcf6 | cc79bf38-7860-4c5c-84eb-30347b694eb6 | 2024-12-13 | Warnings | 2922258b-c665-13d3-e063-6394a90abcf6 cc79bf38-7860-4c5c-84eb-30347b694eb6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.