ARTHRITIS RELIEF CREAM- menthol cream

Arthritis Relief Cream by

Drug Labeling and Warnings

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

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

ARTHRITIS RELIEF CREAM 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50972-275
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	12.5 mg  in 1 mL

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, 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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50972-275-01	57 mL in 1 TUBE; Type 0: Not a Combination Product	10/04/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/04/2017

Labeler - NewMarket Health Products LLC (055293706)