Label: MENTHOL, CAMPHOR cream

  • NDC Code(s): 72937-010-02, 72937-010-04, 72937-010-08, 72937-010-16
  • Packager: SUNSET PAIN RELIEF
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 19, 2023

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.

  • PREGNANCY OR BREAST FEEDING

    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

    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: 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, 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 GOLD 2 OZ

    PAIN RELIEF CREAM 2

  • SUNSET PAIN RELIEF CREAM GOLD 4 OZ

    PAIN RELIEF CREAM 4OZ

  • SUNSET PAIN RELIEF CREAM GOLD 8 OZ

    PAIN RELIEF CREAM 8

  • SUNSET PAIN RELIEF CREAM GOLD 16 OZ

    SUNSET PAIN RELIEF 16

  • INGREDIENTS AND APPEARANCE
    MENTHOL, CAMPHOR 
    menthol, camphor cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-010
    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
    PANTHENOL (UNII: WV9CM0O67Z)  
    ALCOHOL (UNII: 3K9958V90M)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    TRIBUTYL CITRATE (UNII: 827D5B1B6S)  
    GERANIOL (UNII: L837108USY)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    HYDROXYPROLINE (UNII: RMB44WO89X)  
    BUTETH-3 (UNII: OC116GRO69)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    COUMARIN (UNII: A4VZ22K1WT)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)  
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72937-010-04113 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
    2NDC:72937-010-0257 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
    3NDC:72937-010-08227 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
    4NDC:72937-010-16454 g in 1 JAR; Type 0: Not a Combination Product09/15/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/24/2019
    Labeler - SUNSET PAIN RELIEF (067218145)
    Registrant - CHEMCO CORPORATIOM (032495954)