Label: ADVIL TARGETED RELIEF- camphor, capsaicin, menthol, methyl salicylate cream

  • NDC Code(s): 0573-6555-45, 0573-6555-48, 0573-6555-51, 0573-6555-54
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 8, 2024

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  • Active ingredients

    Camphor 3.1%

    Capsaicin 0.025%

    Menthol 10%

    Methyl salicylate 15%

  • Purposes

    Topical analgesic

    Topical analgesic

    Topical analgesic

    Topical analgesic

  • Uses

    • Temporarily relieves minor aches and pains of muscles and joints associated with:
    • arthritis
    • strains
    • simple backache
    • bruises
    • sprains
  • Warnings

    For external use only

    • avoid contact with eyes. If eye contact occurs, rinse thoroughly with water.

    Do not use

    • on wounds or damaged skin
    • with a heating pad
    • if you are allergic to any ingredients in this product

    Ask a doctor before use if you have

    • redness over the affected area

    When using this product

    • do not bandage tightly

    Stop use and ask a doctor if

    • condition worsens or if symptoms last for more than 7 days
    • symptoms clear up and occur again within a few days
    • rash, itching or skin irritation develops

    If pregnant or breast-feeding,ask a health professional before use

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • use only as directed
    • adults and children 12 years and older: apply to affected area not more than 3 to 4 times daily
    • children under 12 years of age: consult your doctor
    • wash hands after applying
  • Other information

    • store between 20-25°C (68-77°F)
  • Inactive ingredients

    carbomer homopolymer, cetyl alcohol, cetyl esters wax, emulsifying wax, oleth-3-phosphate, purified water, sodium hydroxide, stearic acid

  • Questions or comments?

    call toll-free 1-800-88-ADVIL

    Additional information

    DEEP PENETRATING RELIEF

    BACK & BODY ACHES

    ARTHRITIS & JOINT PAIN

    SPRAINS & STRAINS

    SORE MUSCLES

    STARTS WORKING ON CONTACT

    FOR UP TO 8 HOURS OF POWERFUL RELIEF

    UP TO 8 HRS

    HOW TO USE

    Clean and dry affected area

    Remove cap

    Gently squeeze to dispense cream

    Massage cream into skin

    Starts to soothe on contact

    Do Not Use if tube seal under cap is broken or missing.

    Distributed by: Haleon, Warren, NJ 07059

    ©2023 Haleon group of companies or its licensor.

    Trademarks are owned by or licensed to the Haleon group of companies.

    For most recent product information, visit www.Advil.com

    Made in Canada

  • PRINCIPAL DISPLAY PANEL

    NEW HALEON
    DOES NOT CONTAIN THE SAME ACTIVE INGREDIENT AS ADVIL
    Advil

    TARGETED

    RELIEF

    PAIN RELIEVING CREAM

    4 POWERFUL PAIN FIGHTING INGREDIENTS

    Arthritis & Joint Pain

    Sprains & Strains

    Back & Body aches

    Sore Muscles

    FOR EXTERNAL USE ONLY

    NET WT. 65 g (2.3 oz)

    206239 Front

    206239 Advil Targeted Relief 65 g (2.3 oz)
  • INGREDIENTS AND APPEARANCE
    ADVIL TARGETED RELIEF 
    camphor, capsaicin, menthol, methyl salicylate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0573-6555
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)31 mg  in 1 g
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.25 mg  in 1 g
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM100 mg  in 1 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE150 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CETYL ESTERS WAX (UNII: D072FFP9GU)  
    ISOCETYL STEARATE (UNII: 3RJ7186O9W)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0573-6555-541 in 1 CARTON03/06/2024
    165 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:0573-6555-451 in 1 CARTON03/06/2024
    271 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
    3NDC:0573-6555-483 g in 1 POUCH; Type 0: Not a Combination Product03/06/2024
    4NDC:0573-6555-511 in 1 CARTON03/06/2024
    4113.4 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/06/2024
    Labeler - Haleon US Holdings LLC (079944263)
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