Label: CORISIN ARTHRITIS PAIN RELIEF- capsaicin, menthol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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  • CORISIN ARTHRITIS PAIN RELIEF GEL


  • Active ingredient

    Capsaicin 0.025% Menthol 10%

    Purpose

    Topical Analgesic

  • Uses

    For temporary relief of minor aches and pains associated with

    • Simple back ache
    • Arthritis
    • Sprains
    • Cramps
  • For external use only


    When using this product

    • Read inside of carton before using
    • Use only as directed
    • Do not bandage tightly or cover treated areas
    • Do not use with heating pad
    • Avoid contact with eyes and mucous membranes
    • Do not apply to wounds or damaged, broken or irritated skin
    • A mild burning sensation may occur.  If severe burning sensation occurs, discontinue use immediately
    • If symptoms persist for more than seven days, discontinue and consult physician

    Keep out of reach of children

    If swallowed, consult physician

    If pregnant or breast feeding

    contact physician prior to use.

  • Directions


    Adult and children over 18 years:

    • Apply directly to effected area.  Repeat as necessary, but do not use more than 3-4 times daily.
  • Other Ingredients

    Allantoin, Aloe Barbadensis (Aloe Vera) Juice, Aqua (Deionized Water), Carbomer, DMDM Hydrantoin, Glycerin, Methyl Paraben, Polysorbate-20, Propyl Paraben, Glycol, Triethanolamine.

  • CORISIN ARTHRITIS PAIN RELIEF GEL 1oz/28.3g (65121-498-01)

    Corisin Outer
    Corisin Inner


  • INGREDIENTS AND APPEARANCE
    CORISIN ARTHRITIS PAIN RELIEF 
    capsaicin, menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-498
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.025 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65121-498-011 in 1 BOX02/09/2017
    128.3 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/21/2014
    Labeler - Pure Source, LLC (080354456)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source, LLC080354456manufacture(65121-498)
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