Label: NUPHARMISTO TATTOO NUMBING CREAM 80G- lidocaine cream

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

Drug Label Information

Updated May 1, 2024

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

  • Active Ingredient

    active ing

  • ask doctor

    ask doctor

  • Warning do not use if

    do not use if

  • Keep out of reach of children

    No children

  • if pregnant or breast feeding

    if pregnant

  • Purpose

    purpose

  • questions

    questions

  • Stop use warnings

    warnings

  • When using

    when using

  • Directions

    directions

  • inactive Ingredients

    inactive

  • warnings sections

    warnings1

  • How to use it correctly

    how to use

  • Label

    label

  • bottle label

    label2

  • INGREDIENTS AND APPEARANCE
    NUPHARMISTO TATTOO NUMBING CREAM 80G 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71331-116
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.7 g  in 100 g
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    ALLANTOIN (UNII: 344S277G0Z)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    EMU OIL (UNII: 344821WD61)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71331-116-0480 g in 1 PACKAGE; Type 0: Not a Combination Product05/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/01/2024
    Labeler - Orange Lab, Inc (004862271)