Label: QR PAIN- analgesic cream

  • NDC Code(s): 73180-075-00, 73180-075-01
  • Packager: MARYHELENE ENTERPRISES INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 17, 2025

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  • DRUG FACTS

  • Active Ingredient

    Mannitol 30%

    Menthol 1.25%

  • Purpose

    Topical Analgesic

  • Uses

    for the temporary relief of pain.

  • Warnings

    For external use only.

  • When using this product

    • do not bandage tightly
    • avoid contact with the eyes
    • do not apply to wounds or damaged skin
    • do not use with heating pads or other heating devices
    • as with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product
    • do not use in large quantities, particularly over raw surfaces or blistered areas.
  • Stop use and ask a doctor if

    Condition worsens or if symptoms persist for more than 7 days or 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 no more than 3-4 times a day. Children under 12 years of age: do not use, contact a doctor.

  • Other Information

    Protect this product from excessive heat and direct sun.

  • Inactive Ingredients

    Lecithin, Ethylhexylglycerin, Ceteareth 20, Glyceryl stearate, Octyldodecanol, Phenoxyethanol, Propylene glycol, Isopropyl Palmitate, Caprylic/Capric triglyceride, Dimethicone, Polyethylene glycol 100 stearate, Water, Cetearyl alcohol.

  • Questions or Comments?

    1-833-772-7326 (1 833 QR CREAM) or visit www.qrcream.com

  • QR PAIN CREAM 75g (NDC 73180-075-00)

    QR Cream

  • INGREDIENTS AND APPEARANCE
    QR PAIN 
    analgesic cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73180-075
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MANNITOL (UNII: 3OWL53L36A) (MANNITOL - UNII:3OWL53L36A) MANNITOL30 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.25 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73180-075-011 in 1 BOX08/01/2019
    1NDC:73180-075-0075 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/01/2019
    Labeler - MARYHELENE ENTERPRISES INC (203935056)
    Registrant - MARYHELENE ENTERPRISES INC (203935056)
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