ARTHRIPAIN RELIEF- menthol cream

ArthriPain Relief by

Drug Labeling and Warnings

ArthriPain Relief by is a Otc medication manufactured, distributed, or labeled by NDI Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                                                            Purpose

Menthol 1.25%.................................................................Pain relieving cream

PURPOSE

Use  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

Directions

• Adult and children 2 years of age and older: Apply to affected area not more than  3 to 4 times daily.
• Children under 2 years of age: Consult a physician.
  

INACTIVE INGREDIENT

Inactive Ingredients: aloe vera gel, cetyl alcohol, cetyl esters
(proprietary blend of esterfied fatty acids)(7.5%), cinnamon oil,
eucalyptus oil, glyceryl stearate, grape seed oil, hypromellose, jojoba
oil, peppermint oil, potassium sorbate, purified water, squalane, stearic
acid, stearyl alcohol, tea tree oil, vegetable glycerin, wintergreen oil.

PRINCIPAL DISPLAY PANEL

ArthriPain packaging

INGREDIENTS AND APPEARANCE

ARTHRIPAIN RELIEF 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50972-278
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A)	Menthol	12.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 (UNII: 3NXW29V3WO)
JOJOBA OIL (UNII: 724GKU717M)
PEPPERMINT OIL (UNII: AV092KU4JH)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50972-278-01	57 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/01/2010

Labeler - NDI Solutions LLC (828825989)