MOTION MEDICINE- menthol cream

Motion Medicine by

Drug Labeling and Warnings

Motion Medicine by is a Otc medication manufactured, distributed, or labeled by Entreprises ImportFAB Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients (percent by weight)

Menthol 4.0% 

Camphor 4.0%

Purpose

Analgesic (Pain reliever)

Uses

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

Warnings

• Avoid getting into eyes or on mucous membranes.
• If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

Do not apply 

• to wounds or damaged skin. Do not bandage tightly.

Keep out of the reach of children

• Use only as directed.
• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Adults and children 12 years of age or older: Rub this soothing cream on the affected area not more than 3 to 4 times daily.
• Children under the age of 12: Do not use, consult a doctor.

Inactive ingredients

Alcohol denatured, caprylyl glycol, cetyl alcohol, chondroitin sulphate, eucalyptus oil, glucosamine sulphate, glycerin, glycol stearate, grape seed oil, methylsulfonyl methane (MSM), oil of lavender, oil of wintergreen, phenoxyethanol, polysorbate-20, sepigel 305 component, sorbic acid, steareth-100, stearyl alcohol, thymol, urea, vitamin E, water purified.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOTION MEDICINE 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62973-809
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	40 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETYL ALCOHOL (UNII: 936JST6JCN)
EUCALYPTUS OIL (UNII: 2R04ONI662)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCOL STEARATE (UNII: 0324G66D0E)
GRAPE SEED OIL (UNII: 930MLC8XGG)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
LAVENDER OIL (UNII: ZBP1YXW0H8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
SORBIC ACID (UNII: X045WJ989B)
STEARETH-100 (UNII: 4OH5W9UM87)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
THYMOL (UNII: 3J50XA376E)
UREA (UNII: 8W8T17847W)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62973-809-12	120 g in 1 TUBE; Type 0: Not a Combination Product	01/27/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/27/2018

Labeler - Entreprises ImportFAB Inc. (248586117)