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 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

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

  • 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, 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 4 oz TUBE LIMITED EDITION

    pain relief 2000

  • 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
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)3 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    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)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    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)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    COMFREY (UNII: D05HXK6R3G)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72937-310-42113 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 DrugM01703/04/2021
    Labeler - SUNSET NOVELTIES, INC (067218145)
    Registrant - CHEMCO CORPORATION (032495954)
    Establishment
    NameAddressID/FEIBusiness Operations
    CHEMCO CORPORATION032495954manufacture(72937-310)