Label: NUPHARMISTO- lidocaine cream

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

Drug Label Information

Updated February 28, 2024

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  • Drug Facts

    Drug facts - active

  • Purpose

    Local Anesthetic

    Uses

  • Warnings

    Warnings

  • When using this product

    when using this product

  • Stop use and ask a doctor if

    pregnant

  • Keep out of reach of children

    keep out of reach of children

  • How to use it correctly?

    How to use it correctly?

  • Inactive Ingredients

    Inactive ingredients

  • Other information : storage

    Other information

  • Directions for use

    Directions

  • Active ingredient and directions

    Active Ingredientdirections

  • Usage section

    Usage

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  • INGREDIENTS AND APPEARANCE
    NUPHARMISTO 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71331-113
    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) LIDOCAINE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    EMU OIL (UNII: 344821WD61)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)  
    SUNFLOWER OIL UNSAPONIFIABLES (UNII: T7ZE2WA4MB)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71331-113-0560 g in 1 PACKAGE; Type 0: Not a Combination Product03/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01503/01/2024
    Labeler - Orange Lab, Inc (004862271)
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