Minted Leaf Cold Therapy Relief Foot gel

Minted Leaf Cold Therapy Relief Foot by

Drug Labeling and Warnings

Minted Leaf Cold Therapy Relief Foot by is a Otc medication manufactured, distributed, or labeled by MMG Consumer Brands, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MINTED LEAF COLD THERAPY RELIEF FOOT- menthol gel 
MMG Consumer Brands, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Minted Leaf Cold Therapy Relief Foot gel

Drug Facts

Active ingredient

Menthol 16%

Purpose

Topical Analgesic

Uses:

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

Warnings:

For external use only.

Do not use

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

When using this product

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

Stop use and ask a doctor if

  • 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.

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

If pregnant or breastfeeding,

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

Directions:

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

Inactive ingredients:

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:

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

Questions?

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

Package Labeling:

Bottle4

MINTED LEAF COLD THERAPY RELIEF FOOT 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73102-144
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL160 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ARNICA MONTANA WHOLE (UNII: O80TY208ZW)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PETROLATUM (UNII: 4T6H12BN9U)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
XANTHAN GUM (UNII: TTV12P4NEE)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
UREA (UNII: 8W8T17847W)  
CORN (UNII: 0N8672707O)  
PROPANEDIOL (UNII: 5965N8W85T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73102-144-0389 mL in 1 TUBE; Type 0: Not a Combination Product05/08/202012/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/08/202012/31/2021
Labeler - MMG Consumer Brands, LLC (117036455)

Revised: 1/2022
Document Id: d5871ab7-796b-ad6d-e053-2995a90ab2e6
Set id: 8d4276f2-2e08-49cc-af94-45e32cca88ae
Version: 2
Effective Time: 20220114