Label: MENTHOL, CAMPHOR cream

  • NDC Code(s): 70947-103-02
  • Packager: Worldwide Cosmetics, Inc
  • 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 December 14, 2022

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

  • ACTIVE INGREDIENT

    Menthol 10%
    Camphor 3%

  • PURPOSE

    External Analgesic
    Pain Relieving

  • USES:

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

  • WARNINGS

    Use only as directed. For external use only. Do not bandage tightly. Do not use with heating pad,
    pack, wrap, hot water bottle or any heating element. Keep away from children. Package not child
    resistant. In case of accidental ingestion, contact doctor immediately. If prone to allergic reaction to
    the product, consult to a doctor before using.

  • WHEN USING

    Avoid contact with eyes, mucous membranes, rashes, wounds or damaged skin. Do not apply on
    nose and genital area. If rash, redness or itchiness results; discontinue use and consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep away from children. Package not child
    resistant. In case of accidental ingestion, contact doctor immediately.

  • DIRECTIONS:

    Adults and children over 12 years of age; apply a thin layer to 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 unless directed by doctor/physician

  • OTHER INFORMATION:

    Store at room temperature 15° - 30°C (59° - 86°F)

  • INACTIVE INGREDIENT

    Aqua, Ethyl Alcohol, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Paraffinum Liquidum, Cetyl
    Alcohol, Dimethicone, Glyceryl Stearate, Tocopheryl Acetate, Propylene Glycol, Glycereth-26,
    Caprylic/Capric Triglyceride, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Stearyl
    Alcohol, Polysorbate 20, Diazolidinyl Urea, Triethanolamine, Cannabidiol, Methylparaben,
    Propylparaben, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol,
    Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Sodium Benzotriazolyl Butylphenol
    Sulfonate, Buteth-3, Tributyl Citrate, FD&C Blue # 1 (CI 42090), FD&C Yellow #5 (CI 19140).

  • ETERNAL PAINLESS WITH CBD OIL 3000 2 fl oz

    PAINLESS WITH CBD 3000

  • INGREDIENTS AND APPEARANCE
    MENTHOL, CAMPHOR 
    menthol, camphor cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70947-103
    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
    SODIUM COCOYL WHEAT AMINO ACIDS (UNII: JW3VT57I11)  
    WATER (UNII: 059QF0KO0R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    TRIBUTYL CITRATE (UNII: 827D5B1B6S)  
    BUTETH-3 (UNII: OC116GRO69)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYPROLINE (UNII: RMB44WO89X)  
    SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    ALCOHOL 95% (UNII: 7528N5H79B)  
    ACRYLAMIDE (UNII: 20R035KLCI)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70947-103-0257 g in 1 JAR; Type 0: Not a Combination Product05/25/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/22/2022
    Labeler - Worldwide Cosmetics, Inc (013176366)
    Registrant - Chemco Corporation (032495954)
    Establishment
    NameAddressID/FEIBusiness Operations
    Chemco Corporation032495954manufacture(70947-103)