Label: ALFLEXIL ZERO PAIN- camphor, lidocaine hcl, menthol gel

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

Drug Label Information

Updated September 14, 2023

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

  • ACTIVE INGREDIENT

    Camphor 0.5%

    Lidocaine 4%

    Menthol 1%

  • PURPOSE

    Topical Analgesic

  • Use

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

  • 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 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.
    Do not use in large quantities, particularly over raw surfaces or blistered areas.
    If you experience an allergic reaction, discontinue use and consult a physician.

    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 area to be.
    Massaged in a 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 SAFETY INFORMATION

    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, Arnica Montana Flower Extract, Ceteareth-20, Propylene Glycol, Triethanolamine, Carbomer, Glycerin, Methyl Salicylate, Sodium Chondroitin Sulfate, Disodium EDTA, Glucosamine Sulfate, Tocopheryl Acetate, Rosmarinus Officinalis (Rosemary) Extract, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue No.1 (CI 42090).

  • QUESTIONS

    +1(305)597-6410

  • ALFLEXIL ZERO PAIN ROLL-ON

    ALFLEXIL ZERO PAIN

  • INGREDIENTS AND APPEARANCE
    ALFLEXIL ZERO PAIN 
    camphor, lidocaine hcl, menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49283-145
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.5 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49283-145-0390 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/18/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/18/2023
    Labeler - CHEMCO CORPORATION (032495954)