MINTED LEAF COLD THERAPY FOOT RELIEF WITH CBD AND MENTHOL- menthol gel 
MMG Consumer Brands, LLC

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MINTED LEAF Cold Therapy Foot Relief with CBD + Menthol Gel

Drug Facts

Active ingredient

Menthol 16.00%

Purpose

Topical Analgesic

Indications

Warnings:

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

Additional Information

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:

Label

MINTED LEAF COLD THERAPY FOOT RELIEF WITH CBD AND MENTHOL 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73102-064
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL160 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ARNICA MONTANA (UNII: O80TY208ZW)  
CANNABIS SATIVA WHOLE (UNII: B5ONF538PB)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PETROLATUM (UNII: 4T6H12BN9U)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
UREA (UNII: 8W8T17847W)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73102-064-0085 g in 1 TUBE; Type 0: Not a Combination Product08/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/01/2019
Labeler - MMG Consumer Brands, LLC (117036455)

Revised: 11/2023
Document Id: 097502bf-724b-dd2b-e063-6394a90a7520
Set id: cc79bf38-7860-4c5c-84eb-30347b694eb6
Version: 2
Effective Time: 20231105
 
MMG Consumer Brands, LLC