Label: RITE AID ULTRA STRENGTH MUSCLE RUB- methyl salicylate 30.0%, camphor 4.0%, menthol 10.0% cream

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

Drug Label Information

Updated December 18, 2024

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  • Active Ingredient

    Camphor 4%

    Menthol 10%

    Methyl salicylate 30%

  • SPL UNCLASSIFIED SECTION

  • Purpose

    Topical Analgesic

    Topical Analgesic

    Topical Analgesic

  • Directions

    temporarily relieves the minor aches and pains of muscles and joints associated with:

    • simple backache
    • arthritis
    • strains
    • bruises
    • sprains
  • Warnings

    For external use only.

  • Do not Use

    • on wounds or damaged skin
    • with a heating pad
    • on a child under 12 years of age with arthritis-like conditions
  • Ask Doctor

    Ask a doctor before use if you have redness over affected area

  • When Using Section

    • use only as directed
    • avoid contact with eyes or mucous membranes
    • do not bandage tightly
  • Stop use and ask a doctor if

    • condition worsens
    • symptoms last 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. (1-800-222-1222)

  • Directions

    • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 12 years of age: consult a physician
  • Other Information

    • store at 20° to 25°C (68° to 77°F)
    • do not use if tube seal under cap is broken
  • Inactive Ingredients

    carbomer homopolymer type C, cetostearyl alcohol, cetyl alcohol, glycerine monostearate, peg-100 stearate, Phenoxyethanol, polysorbate 60, sodium benzoate, stearic acid, trolamine, water

  • Questions

    www.riteaid.com

  • Rite Aid Ultra Strength Muscle Rub

    label

  • INGREDIENTS AND APPEARANCE
    RITE AID ULTRA STRENGTH MUSCLE RUB 
    methyl salicylate 30.0%, camphor 4.0%, menthol 10.0% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-9993
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM100 mg  in 1 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)40 mg  in 1 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE300 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYOXYL 100 STEARATE (UNII: YD01N1999R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-9993-11 in 1 CARTON03/01/2023
    1113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/01/2023
    Labeler - Rite Aid Corporation (014578892)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anicare Pharmaceuticals Pvt. Ltd.916837425manufacture(11822-9993)
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