Label: MENTHOL, CAMPHOR cream

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

Drug Label Information

Updated June 4, 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

    Stop use and ask a doctor if
    • 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.

  • PREGNANCY 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 right away.

  • Directions

    Adults and Children over 12 years
    • Apply a thin layer to the affected area and rub gently not more than 3 to 4 times a day. • Wash hands with soap and water after use.
    Children under 12 years of age consult a doctor

  • INACTIVE INGREDIENT

    Water (Aqua), Paraffinum Liquidum, Alcohol Denat, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Glycereth-26, Tocopheryl Acetate, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Cannabis Sativa Seed Oil, Stearyl Alcohol, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Polysorbate 20, Triethanolamine, Fragrance (Parfum), Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Sodium Benzotriazolyl Butylphenol Sulfonate, Buteth-3, Tributyl Citrate, Cannabidiol, FD&C Blue No.1 (CI 42090), Linalool, Limonene, Benzyl Benzoate, Coumarin, Geraniol.

  • SUNSET PAIN RELIEF CREAM TUBE 8 FL OZ

    PAIN RELIEF GOLD 8OZ

  • INGREDIENTS AND APPEARANCE
    MENTHOL, CAMPHOR 
    menthol, camphor cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-310
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 g
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    TRIBUTYL CITRATE (UNII: 827D5B1B6S)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    HYDROXYPROLINE (UNII: RMB44WO89X)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) (UNII: M4PPW69Y4H)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    BUTETH-3 (UNII: OC116GRO69)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    ALCOHOL (UNII: 3K9958V90M)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    COUMARIN (UNII: A4VZ22K1WT)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    COMFREY (UNII: D05HXK6R3G)  
    GERANIOL (UNII: L837108USY)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72937-310-08226 g in 1 TUBE; Type 0: Not a Combination Product03/04/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/04/2021
    Labeler - SUNSET NOVELTIES, INC (067218145)