KENS PAIN AND ARTHRITIS FORMULA- menthol liquid 
EEZAWAY RELIEF INC

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Kens Pain and Arthritis Formula

Drug Facts

Active Ingredient:

Menthol 2.75%

Purpose

Topical Analgesic

Uses

temporarily relieves minor pain associated with:

• arthritis • simple backache • muscle strains • sprains • bruises • cramps

Warnings

For external use only

When using this product • use only as directed • do not bandage tightly or use with heating pad • avoid contact with eyes and mucous membranes • do not apply to wounds or damaged, broken or irritated skin • a transient burning sensation or redness may occur upon application but generally disappears in several days • if severe burning sensation occurs, discontinue use immediately • do not expose the area treated with product to heat or direct sunlight

Stop use and ask a doctor if • Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

Flammable • keep away from fire or flame

If pregnant or breast-feeding, ​ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children over 12 years: • shake well before using every time • apply generously to affected area • massage into painful area until thoroughly absorbed into skin • repeat as necessary, but no more than 3 to 4 times daily

MAKE SURE YOU SHAKE BOTTLE BEFORE EVERY TIME YOU APPLY IT

children 12 years or younger: ask a doctor

Inactive Ingredients

Emu Oil, Carbomer, Full Spectrum Hemp Oil (Cannabidiol), PPG-20 Methyl Glucose Ether, Isopropyl Alcohol USP, Oleth-10, PEG-75 Lanolin, Purified Water, Sodium Thiosulfate Pentahydrate, Tincture of Iodine.

Pain Relief CBD Roll-On

5,000mg of CBD

for temporary relief of minor aches and pains associated with

ARTHRITIS SIMPLE ACHES AND PAINS
SORE AND TIRED MUSCLES

SHAKE WELL BEFORE EVERY USE

Eezaway Relief Inc.

Please Call 800-898-3755 www.kenspainrelief.com

MADE IN USA

Packaging

image description

KENS PAIN AND ARTHRITIS FORMULA 
menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69678-143
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM2.75 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
EMU OIL (UNII: 344821WD61)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
PPG-20 METHYL GLUCOSE ETHER (UNII: 3WV1T97D3K)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
OLETH-10 (UNII: JD797EF70J)  
PEG-75 LANOLIN (UNII: 09179OX7TB)  
WATER (UNII: 059QF0KO0R)  
SODIUM THIOSULFATE (UNII: HX1032V43M)  
IODINE (UNII: 9679TC07X4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69678-143-0388 mL in 1 BOTTLE; Type 0: Not a Combination Product03/05/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/05/2024
Labeler - EEZAWAY RELIEF INC (109456638)

Revised: 10/2021
Document Id: 616f23fd-bf08-4a36-809f-c5a6227443a4
Set id: 35834473-3ad5-41ec-a110-e742aa7e2ee4
Version: 1
Effective Time: 20211021
 
EEZAWAY RELIEF INC