MINTED LEAF COLD THERAPY FOOT RELIEF WITH CBD AND MENTHOL- menthol gel

MINTED LEAF Cold Therapy Foot Relief with CBD and Menthol by

Drug Labeling and Warnings

MINTED LEAF Cold Therapy Foot Relief with CBD and Menthol by is a Otc medication manufactured, distributed, or labeled by MMG Consumer Brands, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

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:

INGREDIENTS AND APPEARANCE

MINTED LEAF COLD THERAPY FOOT RELIEF WITH CBD AND MENTHOL 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73102-064
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	160 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73102-064-00	85 g in 1 TUBE; Type 0: Not a Combination Product	08/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/01/2019

Labeler - MMG Consumer Brands, LLC (117036455)