TRIMOTION PAIN RELIEF- menthol, methyl salicylate cream

TriMotion Pain Relief by

Drug Labeling and Warnings

TriMotion Pain Relief by is a Otc medication manufactured, distributed, or labeled by NatureMed, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients:

Menthol 2.50%

Methyl Salicylate 10%

Purpose

Topical Analgesic

Uses:

For the temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.

Warnings:

For external use only.

When using this product

• use only as directed
• do not bandage tightly or use with aheating pad
• do not apply to wounds or damaged skin
• avoid contact with eyes or mucous membranes.

Stop use and ask a doctor if

• condition worsens
• irritation develops
• redness is present
• symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breastfeeding

ask a health professional prior to use.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control immediately.

Directions:

• Adults and children 12 years of age or older: Apply to affected area not more than three to four times daily.
• Children under 12 years of age: consult a physician.

Other Information:

Store at room temperature.

Inactive ingredients:

Aloe Barbadensis (Aloe Vera) Extract, Anthemis Nobilis (Chamomile) Flower Extract, Aqua (Deionized Water), Arnica Montana (Arnica) Extract, Boswellia Serrata Extract, Calendula Officinalis (Marigold) Flower Extract, Cetearyl Olivate, Chondroitin Sulfate, Cucumis Sativus (Cucumber) Fruit Extract, Dimethyl Sulfone (MSM), Emu Oil, Gluconolactone, Glucosamine Sulfate, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Melaleuca Alternifolia (Tea Tree) Leaf oil, Propanediol, Salix Alba (Willow) Bark Extract, Sodium Benzoate, Sorbitan Olivate, Xanthan
Gum.

Questions or comments?

Call 1-800-218-1379

Package Labeling:

INGREDIENTS AND APPEARANCE

TRIMOTION PAIN RELIEF 
menthol, methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 45632-736
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	25 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	100 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CUCUMBER (UNII: YY7C30VXJT)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EMU OIL (UNII: 344821WD61)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
TEA TREE OIL (UNII: VIF565UC2G)
PROPANEDIOL (UNII: 5965N8W85T)
SALIX ALBA BARK (UNII: 205MXS71H7)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITAN OLIVATE (UNII: MDL271E3GR)
XANTHAN GUM (UNII: TTV12P4NEE)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA (UNII: O80TY208ZW)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CETEARYL OLIVATE (UNII: 58B69Q84JO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 45632-736-01	1 in 1 BOX	04/06/2016
1		57 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/06/2016

Labeler - NatureMed, Inc (186976093)