ARTHRITIS RELIEF CREAM- menthol cream 
NewMarket Health Products 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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Arthritis Relief Cream

Active Ingredient section

 Menthol, Unspecified Form   1.25%

Purpose

Topical Analgesic

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with:
• Simple backache
• Arthritis
• Strains
• Bruises
• Sprains

Warnings

For external use only.

Do not use

• On wounds or damaged skin

When using this product
• Avoid contact with eyes or mucous membranes
• Do not bandage tightly

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily.
• Children under 12 years of age: Consult a physician.

Other Information.

Questions? Need to refill? 1-800-895-2108

Inactive Ingredients

Aloe Vera Gel, Cetyl Alcohol, Cetyl Esters (proprietary blend of esterified fatty acids), Cinnamon Oil, Eucalyptus Oil, Glyceryl Stearate, Grape Seed Oil, Hypromellose, Jojoba Oil, Olive Oil, Peppermint Oil, Phenoxyethanol, Potassium Sorbate, Purified Water, Sodium Benzoate, Squalane, Stearic Acid, Stearyl Alcohol, Tea Tree Oil, Vegetable Glycerin, Wintergreen Oil.

Product Image

image description

ARTHRITIS RELIEF CREAM 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50972-275
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM12.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CETYL ESTERS WAX (UNII: D072FFP9GU)  
CINNAMON OIL (UNII: E5GY4I6YCZ)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
GRAPE SEED OIL (UNII: 930MLC8XGG)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
JOJOBA OIL (UNII: 724GKU717M)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SQUALANE (UNII: GW89575KF9)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
TEA TREE OIL (UNII: VIF565UC2G)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50972-275-0157 mL in 1 TUBE; Type 0: Not a Combination Product10/04/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/04/2017
Labeler - NewMarket Health Products LLC (055293706)

Revised: 1/2021
Document Id: b9556394-7d28-64aa-e053-2a95a90ad8ff
Set id: 6004a5f1-4f83-47da-8b1e-6d62e41c4c2e
Version: 1
Effective Time: 20210120
 
NewMarket Health Products LLC