Label: PAIN RELIEVING IAMPUR- camphor, menthol, methyl salicylate cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated May 24, 2013

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  • ACTIVE INGREDIENT

    Camphor 4%, Menthol 4%, Methyl Salicylate 11%

  • INDICATIONS & USAGE

    Uses

    Temporarily relieves minor muscle pain, joint pain.  Temporarily relieves pain associated with:  arthritis pain, backache, strains, sprains, and bruises.

  • WARNINGS

    Warnings

    For external use only. Use only as directed.  Do not use on wounds or damaged skin.  When using this product avoid contact with eyes and mucous membranes, do not bandage tightly.  Stop use and consult doctor if condition worsens or symptoms persist for more than 7 days or symptoms clear up and occur again within a few days. 

  • DOSAGE & ADMINISTRATION

    Directions

    Adults and children 12 years of age and older:  use no more than 3 to 4 times daily.  Apply cream to affected  areas and thoroughly massage until penetrated.  Wash hands with soap and water after use.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Acrylates C10-30 alkyl acrylate crosspolymer, Water, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Ceteth-10 Phosphate, Cyclomethicone, Dicetyl Phosphate, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Isopropyl Palmitate, Methylsulfonylmethane (MSM), Phenoxyethanol, Triethanolamine.

  • PURPOSE

    Purpose

    Topical Analgesic.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

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

  • PRINCIPAL DISPLAY PANEL

    Iampur Pain Relief Massager

    Pain Relieving Gel

    label image

  • INGREDIENTS AND APPEARANCE
    PAIN RELIEVING  IAMPUR
    camphor, menthol, methyl salicylate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43493-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) MENTHOL4 g  in 1 g
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)4 g  in 1 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE11 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)  
    DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43493-0002-4120 g in 1 VIAL, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/24/2013
    Labeler - Avaria Health & Beauty Corp (248926979)
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