Label: MENTHOL, CAMPHOR cream

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

Drug Label Information

Updated February 7, 2024

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

  • ACTIVE INGREDIENT

    Camphor 3%

    Menthol 10%

  • PURPOSE

    Topical Analgesic

  • USE

    For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.

  • WARNINGS

    For external use only. · Ask a doctor before use if you have redness over affected area

  • WHEN USING

    Use only as directed.
    Do not bandage tightly.
    Do not use with heating pad, pack, wrap, hot water bottle or any heating element.
    In case of accidental ingestion, contact doctor immediately.

    If prone to allergic reaction to the product, consult to a doctor before using.

  • STOP USE

    Condition worsens.
    Redness is present.
    Irritation develops.
    Symptoms persist for more than 7 days or clear up occur again within a few days.

    You experience signs injury, such as pain, swelling or blistering where the product was applied.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast – feeding

    Ask a health professional before use.

  • DIRECTIONS

    Adults and Children over 12 years

    Apply a small amount on desired area.
    Massage in circular motions until absorbed.
    Repeat as needed, but no more than 3 to 4 times per day.
    Wash hands with soap and water after use.

    Children under 12 years of age: do not use, consult a doctor.

  • OTHER SAFETY INFORMATION

    Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

  • INACTIVE INGREDIENT

    Water (Aqua), Paraffinum Liquidum, Alcohol Denat, Cetearyl Alcohol, Cetyl Alcohol, Stearic Acid, Dimethicone, Glyceryl Stearate, Glycereth-26, Tocopheryl Acetate, Cannabis Sativa Seed Oil, Propylene Glycol, Polysorbate 60, Diazolidinyl Urea, Methylparaben, Propylparaben, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Fragrance (Parfum), Stearyl Alcohol, Polysorbate 20, Triethanolamine, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Aloe Barbadensis Leaf Extract, Glycerin, Sodium Benzotriazolyl Butylphenol Sulfonate, Buteth-3, Tributyl Citrate, Cannabidiol, FD&C Yellow No.5 (CI 19140), Geraniol, Hexyl Cinnamal, Amyl Cinnamal, Citronellol, Hydroxycitronellal, Linalool, Coumarin.

  • SUNSET - JOINT AND MUSCLE PAIN RELIEF CREAM 4 oz TUBE LIMITED EDITION

    TEA TREE 2000

  • INGREDIENTS AND APPEARANCE
    MENTHOL, CAMPHOR 
    menthol, camphor cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-300
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM10 g  in 100 g
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    GERANIOL (UNII: L837108USY)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    COUMARIN (UNII: A4VZ22K1WT)  
    COMFREY LEAF (UNII: DG4F8T839X)  
    BUTETH-3 (UNII: OC116GRO69)  
    AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    HYDROXYPROLINE (UNII: RMB44WO89X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TRIBUTYL CITRATE (UNII: 827D5B1B6S)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ALCOHOL (UNII: 3K9958V90M)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72937-300-42113 g in 1 TUBE; Type 0: Not a Combination Product02/07/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/04/2020
    Labeler - SUNSET NOVELTIES, INC (067218145)