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

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MINTED LEAF Cold Therapy Relief with CBD & Menthol Gel

Drug Facts

Active ingredient

Menthol 4.00%

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:

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arcticum Lappa (Burdock) Root Extract, Arnica Montana Flower Extract, Boswellia Serrata Extract, Camellia Sinensis (Green Tea) Extract, Broad Spectrum Hemp Oil, Copper Sulfate, Ethylhexylglycerin, Ilex Paraguariensis (Yerba Mate’) Extract, Isopropyl Alcohol, Isopropyl Myristate, Melissa Officinalis (Lemon Balm) Extract, Methylsulfonylmethane (MSM), Phenoxyethanol, Sodium Hydroxide, Tocopheryl Acetate (Vitamin E), Zemea (Corn) Propanediol.

Package Labeling:

Label3

MINTED LEAF COLD THERAPY RELIEF WITH CBD AND MENTHOL 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73102-063
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
CANNABIS SATIVA WHOLE (UNII: B5ONF538PB)  
CUPRIC SULFATE (UNII: LRX7AJ16DT)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
MELISSA OFFICINALIS (UNII: YF70189L0N)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73102-063-0085 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-723d-dd2b-e063-6394a90a7520
Set id: 762a1cb2-5430-422f-807a-d2c9fdeacb09
Version: 2
Effective Time: 20231105
 
MMG Consumer Brands, LLC