Label: METHYL SALICYLATE 25% PAIN RELIEVING- methyl salicylate cream

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

Drug Label Information

Updated July 15, 2025

If you are a consumer or patient please visit this version.

  • Active Ingredients:

    Methyl Salicylate 25%

  • Purpose:

    Topical Analgesic

  • Uses:

    ■ For the temporary relief of minor aches and pains of muscle and joints associated with ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

  • Warnings:

    ■ For External Use Only

    ■ Keep this and all other drugs out of the reach of children.

    When using this product

    ■ Avoid contact with eyes ■ Do not bandage tightly ■ Do not apply to wounds or broken skin

    Stop use and ask doctor if

    ■ 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 physician.

  • Directions

    ■ Use only as directed. Adults and children 2 years and older: Apply to affected area no more than 3 to 4 times daily. ■ Children under 2 years of age: Do not use, consult a physician.

  • Other information

    ■ Store at 20°-25°C (68°-77°F) [see USP Controlled Room Temperature].

  • Inactive ingredients:

    Aloe Barbadensis (Aloe Vera) Leaf Juice, Aqua (Purified Water), Borago Officinalis (Borage) Seed Oil, Carbomer, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, DL-Alpha Tocopheryl Acetate, Eucalyptus Globus Leaf Oil, Fructose, Phenoxyethanol, Propylene Glycol, Sodium Hydroxide, Squalane, Stearic Acid, Stearyl Alcohol, Tetrasodium EDTA, Vitis Vinifera (Grape) Seed Oil, Fragrance.

  • Methyl Salicylate 25%

    Manufactured by:
    PureTek Corporation

    Panorama City, CA 91402
    For questions or information
    call toll-free: 877-921-7873

    Label

  • INGREDIENTS AND APPEARANCE
    METHYL SALICYLATE 25%  PAIN RELIEVING
    methyl salicylate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59088-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE250 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CETEARETH-20 (UNII: YRC528SWUY)  
    AQUA (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FRUCTOSE (UNII: 6YSS42VSEV)  
    CETEARYL ALCOHOL (UNII: 2DMT128M1S)  
    VITIS VINIFERA (GRAPE) SEED OIL (UNII: 930MLC8XGG)  
    CARBOMER (UNII: 0A5MM307FC)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TETRASODIUM EDTA (UNII: MP1J8420LU)  
    EUCALYPTUS GLOBULUS LEAF OIL (UNII: 2R04ONI662)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SQUALANE (UNII: GW89575KF9)  
    BORAGO OFFICINALIS SEED OIL (UNII: F8XAG1755S)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59088-014-0660 g in 1 JAR; Type 0: Not a Combination Product06/12/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/12/2025
    Labeler - Puretek Corporation (785961046)