Label: TOPCARE MEDICATED PAIN RELIEVING PATCH 60CT- topcare pain relief patch extra strength patch

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

Drug Label Information

Updated January 26, 2026

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

  • ACTIVE INGREDIENT

    Active ingredients Purpose
    Camphor 3.1%............................................................Topical analgesic
    Menthol 6.0%..............................................................Topical analgesic
    Methyl salicylate 10.0%...............................................Topical analgesic

  • PURPOSE

    Uses
     temporary relief of minor aches and pains of muscles and joints
    associated with:
     arthritis  simple backache  sprains  bruises
     strains

  • WARNINGS

    Warnings
    For external use only.

  • DO NOT USE

    Do not use
     on wounds or damaged skin  with a heating pad
     if you are allergic to any ingredients of this product
     on a child under 12 years of age with arthritis-like conditions

  • OTHER SAFETY INFORMATION

    Allergy alert: If prone to allergic reaction from aspirin or salicylates,
    consult a doctor before use.

  • WHEN USING

    When using this product
     use only as directed
     avoid contact with the eyes, or mucous membranes
     do not bandage tightly
     discontinue use at least 1 hour before a bath or shower
     do not use immediately after a bath or shower

  • STOP USE

    Stop use and ask a doctor if
     condition worsens, or symptoms persist for more than 7 days, or
    clear up and occur again within a few days
     redness is present or irritation or rash develops
     a severe burning sensation occurs

  • PREGNANCY OR BREAST FEEDING

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or
    contact a Poison Control Center (1-800-222-1222) right away.

  • INDICATIONS & USAGE

    Directions
     adults and children 12 years of age and older:
     clean and dry affected area
     remove patch from film
     apply to affected area no more than 3 to 4 times daily
     do not wear patch for more than 4 hours
     children under 12 years of age: consult a doctor

  • STORAGE AND HANDLING

    Other information
     store at room temperature 20-25ºC (68-77º)
     avoid storing product in direct sunlight
     protect product from excessive moisture

  • INACTIVE INGREDIENT

    Inactive ingredients aluminum silicate, butylated
    hydroxytoluene, glyceryl rosinate, lanolin, natural rubber, paraffin,
    polyisobutylene (85000 MW), polyisobutylene (800000 MW),
    styrene-isoprene-styrene block copolymer, titanium dioxide, zinc oxide

  • DOSAGE & ADMINISTRATION

    Questions or comments?

    Call 1-888-423-0139

    Distributed By TOPCO ASSOCIATES LLC

    ITASCA, IL 60143 @TOPCO UNXA0525

    Questions? 1-888-423-0139

    opcare@topco.com www.topcarebrand.com

    MADE IN CHINA

  • PRINCIPAL DISPLAY PANEL

    Topco 2385 CMMS Patch

  • INGREDIENTS AND APPEARANCE
    TOPCARE MEDICATED PAIN RELIEVING PATCH 60CT 
    topcare pain relief patch extra strength patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-750
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL60 mg  in 1 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)31 mg  in 1 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    GLYCERYL ROSINATE (UNII: SD112V492J)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    POLYISOBUTYLENE (800000 MW) (UNII: Y132ZOQ9H7)  
    STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMER (UNII: K7S96QM8DV)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    ALUMINUM SILICATE (UNII: T1FAD4SS2M)  
    POLYISOBUTYLENE (85000 MW) (UNII: 7X53O5S2ZY)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:36800-750-601 in 1 BOX01/26/2026
    11 g in 1 POUCH; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/26/2026
    Labeler - Topco Associates LLC (006935977)