Minted Leaf Cold Therapy Relief Foot gel

Manufacturer
MMG Consumer Brands, LLC
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:26:10

Label at a glance#

ProductMinted Leaf Cold Therapy Relief Foot
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

For the temporary relief of minor foot and ankle discomfort and aches associated with strains, bruises and sprains. Provides rapid cooling relief.

Dosage and administration

Adults: Apply to affected area not more than 3 to 4 times daily.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 16%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

  • For the temporary relief of minor foot and ankle discomfort and aches associated with strains, bruises and sprains.
  • Provides rapid cooling relief.

Warnings:

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • On damaged or broken skin.
  • Do not bandage tightly.
  • If you are allergic to any ingredients in this product.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. Rinse with water to remove.
  • Use only as directed.
  • Wash hands after use.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Rash or irritation develops and lasts.
  • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use. FDA strongly advises against the use of cannabidiol (CBD) in any form during pregnancy or while breastfeeding.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Adults: Apply to affected area not more than 3 to 4 times daily.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water) Arnica Montana Extract, Betaglucan, Broad 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.

Other information:

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun.
  • Do not use if seal is broken or missing.

Questions?

OTC - QUESTIONS SECTION

  • 9171 S. Dixie Hwy, Pinecrest, FL 33156.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73102-14473102-144-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d5871ab7-796b-ad6d-e053-2995a90ab2e68d4276f2-2e08-49cc-af94-45e32cca88ae2022-01-14WarningsExact identifier
spl set id: 8d4276f2-2e08-49cc-af94-45e32cca88ae

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.