ARTHRITIS RELIEF- menthol cream

Arthritis Relief by

Drug Labeling and Warnings

Arthritis Relief by is a Otc medication manufactured, distributed, or labeled by NewMarket Health Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Menthol 1.25%

Purpose

Topical Analgesic

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.

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

Directions

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

Inactive Ingredients:

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

Questions?

1-800-895-2108

Package Labeling:

INGREDIENTS AND APPEARANCE

ARTHRITIS RELIEF 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50972-300
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)
HYPROMELLOSES (UNII: 3NXW29V3WO)
JOJOBA OIL (UNII: 724GKU717M)
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)
METHYL SALICYLATE (UNII: LAV5U5022Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50972-300-01	57 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/29/2017

Labeler - NewMarket Health Products LLC (828825989)