FAST RELIEF ARTROSAMIN- menthol, methyl salicylate cream 
Interfarma Corp

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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FAST RELIEF ARTROSAMIN

DRUG FACTS

Active Ingredient:                             Purpose:

Menthol 2.5%...................................External Analgesic

Methyl Salicylate 15%......................External Analgesic

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains.

Warnings:

Keep out of reach of children to avoid accidental poisoning.

Caution: Discontinue use if excessive irritation of the skin develops. Avoid getting into eyes or mucous membranes. If condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days, or redness is present, or in conditions affecting children under 12 years of age, discontinue use and consult a physician immediately.

Directions

Apply to the affected area. Gently massage into the skin for a few seconds. Adults and children over 12 years of age: apply to the affected area not more than 3 to 4 times daily. Children under 12 years of age need to consult a physician.

Inactive Ingredients:

Acrymalide, Amino Acids, Comfrey Leaf, Cetyl Alcohol, Diazolidinyl Urea, Dimethicone, Glucosamine, Methyl Paraben, MSM (Methylsulfonylmethane), Mineral Oil, Panthenol, Propylene Glycol, Propylparaben, Sodium Pyrrolidone Carboxylate, Stearic Acid, Stearyl Alcohol, Trolamine, Water.

Manufactured for:

Interfarma Corp.

Miami, FL 33186.

FAST RELIEF

ARTROSAMIN

For Temporarily Relieves minor aches and pains soreness, and stiffness associated with simple backaches strains, arthritis and rheumatism.

Net Wt 8 oz (226g)

Made in USA

image description

FAST RELIEF ARTROSAMIN 
menthol, methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69706-0203
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.5 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE15 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ACRYLAMIDE (UNII: 20R035KLCI)  
AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
COMFREY LEAF (UNII: DG4F8T839X)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
GLUCOSAMINE (UNII: N08U5BOQ1K)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PANTHENOL (UNII: WV9CM0O67Z)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69706-0203-9226 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/11/2013
Labeler - Interfarma Corp (884091703)
Registrant - Interfarma Corp (884091703)
Establishment
NameAddressID/FEIBusiness Operations
Interfarma Corp884091703manufacture(69706-0203)

Revised: 10/2015
Document Id: 67b34aa9-c584-4578-83d3-de9ea61d72d5
Set id: 17ee8850-4d78-4e41-84c7-a8f9e4c2cdaf
Version: 1
Effective Time: 20151001
 
Interfarma Corp