Label: MYDERM MEDICAL 5 LIDOCAINE NUMBING ROLL-ON- lidocaine stick

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

Drug Label Information

Updated June 24, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient

    Lidocaine 5%

  • WHEN USING

    When using this product avoid conatct with the eyes or muccous membranes.

  • PURPOSE

    Lidocaine 5% ------------------------------------------------------------Local Anesthetic

  • WARNINGS

    For external use only.

  • STOP USE

    Stop use and ask doctor if condition worsens, or symtoms persist for more than 7 days,or clear up and reoccur again within a few days.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • INACTIVE INGREDIENT

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer

    Aloe Vera Barbadensis Leaft Juice

    Inactive ingredients

    2-animo-2methyl-1propanol

    2-Methylamino-2-methyl-1-propanol

    Cetearyl Alcohol

    Citric Acid

    Dimethicone

    Disodium EDTA

    Ethanol

    Ethyhexylglycerin

    Glyceril Stearate

    Phenoxyethanol

    Potassium Sorbate

    Silicone Gel

    Sodium Benzoate

    Steareth-21

    Water

  • DOSAGE & ADMINISTRATION

    Apply to affected area not more than 3 to 4 times daily

  • INDICATIONS & USAGE

    For external use only

  • PRINCIPAL DISPLAY PANEL

    MyDerm 5 Lidocaine

  • INGREDIENTS AND APPEARANCE
    MYDERM MEDICAL 5 LIDOCAINE NUMBING ROLL-ON 
    lidocaine stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72667-072
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    DIMETHICONE 100 (UNII: RO266O364U)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    ALCOHOL (UNII: 3K9958V90M)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    STEARETH-21 (UNII: 53J3F32P58)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72667-072-0189 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/06/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01503/06/2024
    Labeler - Inspec Solutions (081030372)
    Establishment
    NameAddressID/FEIBusiness Operations
    Inspec Solutions081030372manufacture(72667-072)
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