Label: DZUL - LIDO CREME- lidocaine hcl, menthol lotion

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

Drug Label Information

Updated September 25, 2023

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

  • ACTIVE INGREDIENT

    Lidocaine HCl 4%

    Menthol 1%

  • PURPOSE

    Topical Analgesic

  • USES:

    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.
    Avoid contact with eyes and mucous membranes.
    Do not bandage tightly or use with a heating pad.
    A transient burning sensation or redness may occur upon application but generally disappears in several days.

    Do not apply on large areas of the body or on damaged, broken, or irritated skin.

  • STOP USE AND ASK A DOCTOR IF:

    Redness is present.
    Condition worsens.
    Irritation develops.
    Symptoms persist for more than 7 days or clear up and 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 of age

    Apply a small amount to the affected area.
    Massage 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 unless directed by doctor.

  • OTHER SAFETY INFORMATION

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

  • INACTIVE INGREDIENT

    Water, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Isopropyl Myristate, Glycol Stearate, Stearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Sodium Lauryl Sulfate, Dimethicone, Glycerin, Caprylhydroxamic Acid, Caprylyl Glycol, Eucalyptus Globulus Leaf Oil, Phenoxyethanol, Methylpropanediol, Acrylamide/Sodium Acrylate Copolymer, Paraffinum Liquidum, Trideceth-6, Methylsulfonylmethane, Aloe Barbadensis (Aloe Vera) Leaf Juice, Rosmarinus Officinalis (Rosemary) Oil, Tocopheryl Acetate, Arnica Montana Flower Extract, Salix Alba Bark Extract, Glucosamine Sulfate, Chamomilla Recutita (Matricaria) Flower Extract, Capsicum Annuum Fruit Extract.

  • DZUL - LIDO CREME ROLL-ON

    LIDO CREME

  • INGREDIENTS AND APPEARANCE
    DZUL - LIDO CREME 
    lidocaine hcl, menthol lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83037-041
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALMOND OIL (UNII: 66YXD4DKO9)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    CHAMOMILE (UNII: FGL3685T2X)  
    SALIX ALBA BARK (UNII: 205MXS71H7)  
    CAPSICUM ANNUUM WHOLE (UNII: 7FKZ3QQQ1F)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83037-041-0271 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/02/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/17/2022
    Labeler - Caball Sales, Inc. (047422138)