Label: AY BENDITO - CBD- camphor, menthol gel

  • NDC Code(s): 72524-064-04, 72524-064-40
  • Packager: AY BENDITO INTERNATIONAL, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 1, 2024

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

  • ACTIVE INGREDIENT

    Camphor ………………. 6%

    Menthol …………….…. 4%

  • PURPOSE

    Topical Analgesic

  • INDICATIONS & USAGE

    Aid for temporary local relief of minor pain in muscles or joints.

  • WARNINGS

    For external use only.

  • WHEN USING

    Use only as directed
    Do not bandage tightly or use with a heating pad
    Avoid contact with eyes and mucous membranes
    Do not apply to wounds or damaged, broken or irritated skin
    A transient burning sensation or redness may occur upon application but generally disappears in several days
    If you experience an allergic reaction, discontinue use and consult a doctor

    Do not expose the area treated with product to heat or direct sunlight.

  • 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 of age:

    Apply a small amount on the affected area.
    Massage in circular motion, let set for a few seconds.
    Repeat as necessary, but no more than 3 to 4 times daily.
    Children under 12 years of age: do not use, consult a doctor.

  • OTHER INFORMATION

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

  • INACTIVE INGREDIENT

    Water (Aqua), Alcohol Denat, Glycerin, Paraffinum Liquidum, Triethanolamine, Arnica Montana Flower Extract, Polysorbate 20, Carbomer, Methyl Salicylate, Sodium Chondroitin Sulfate, Glucosamine Sulfate, Rosmarinus Officinalis (Rosemary) Extract, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue No.1 (CI 42090).

  • QUESTION OR COMMENTS?

    Call: +1-787-421-6423

  • AY BENDITO - CBD OIL JAR

    CBD JAR

  • AY BENDITO - CBD OIL TUBE

    CBD TUBE

  • INGREDIENTS AND APPEARANCE
    AY BENDITO - CBD 
    camphor, menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72524-064
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL4 g  in 100 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)6 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    LAURETH-7 (UNII: Z95S6G8201)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ALCOHOL (UNII: 3K9958V90M)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Product Characteristics
    Colorgreen (Light) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72524-064-40113 g in 1 JAR; Type 0: Not a Combination Product02/15/2024
    2NDC:72524-064-04113 g in 1 TUBE; Type 0: Not a Combination Product02/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/15/2024
    Labeler - AY BENDITO INTERNATIONAL, INC (081332094)