CBD MENTHOL PAIN RELIEF  FAST ACTING PAIN ROLLER- menthol, unspecified form gel 
Global Products Group, 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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CBD Menthol Pain Relief
Fast Acting Pain Roller

Drug Facts

Active Ingredient

Natural Menthol, USP (8.5%)

Purpose

Topical Analgesic

Uses

Temporarily relieves muscle and joint pain associated with arthritis

Warnings

For external use only: Flammable: Keep away from excessive heat or open flame

  • Ask a doctor before use if you have sensitive skin or if you are taking any blood thinners

  • When using this product: Do not use on wounds or irritated skin
  • Do not bandage tightly or use with a heating pad
  • Wash hands after use with cool water

  • If pregnant or breastfeeding: Ask a health professional before use

  • Keep out of reach of children. If accidentally swallowed, contact a doctor or poison control center immediately

  • Stop use and ask a doctor: If condition worsens or if pain persists for more than 7 days, or clears up, then reoccurs within a few days.

Directions

Use only as directed

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Serrata Extract, Camphor, Carbomer, Chondroitin Sulfate, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Ilex Paraguariensis Extract, Isopropyl Alcohol, Methyl Sulfonylmethane, Peppermint Oil, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Purified Water, Triethanolamine

Other Information

Questions or comments?

Call (877) 383-2334. Store in a cool dry place with the cap tightly closed. Note: Because this product contains natural ingredients, color may vary.

Distributed by FORE

PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

FORE

150MG
CBD
Menthol
PAIN
RELIEF
Fast-Acting Pain Roller

Net Wt. 3 fl oz (88 ml)

Principal Display Panel - 88 ml Bottle Label
CBD MENTHOL PAIN RELIEF   FAST ACTING PAIN ROLLER
menthol, unspecified form gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72593-158
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM85 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ARNICA MONTANA WHOLE (UNII: O80TY208ZW)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)  
GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N)  
GLYCERIN (UNII: PDC6A3C0OX)  
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72593-158-1288 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/05/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34810/05/2020
Labeler - Global Products Group, LLC (081371764)

Revised: 1/2022
Document Id: ab0d2fbf-ceda-4085-b84b-4f436d2e4ae5
Set id: 0382e535-3d6c-40fc-bf85-632f0b675c30
Version: 2
Effective Time: 20220125
 
Global Products Group, LLC