Label: LIPROTEK- petrolatum, lidocaine ointment

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

Drug Label Information

Updated October 19, 2023

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  • Uses:

    TEMPORARY RELIEF OF PAIN and/or ITCHING FROM FEVER BLISTERS and COLD SORES

  • DRUG FACTS

  • Active Ingredient

    Petrolatum (white) 61%

    Lidocaine 0.6%

    PURPOSE

    Skin Protectant

    External or Topical Analgesic

  • Uses:

    TEMPORARY RELIEF OF PAIN AND/OR ITCHING FROM FEVER BLISTERS AND COLD SORES

  • WARNING:

    Keep away from children.

    Do not use

    if allergic tp any of the ingredients. If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days then discontinue use of this product and cunsult a doctor.

  • INGREDIENTS:

       Simmondisa Chinensis (Jojoba) Seed Oil, Lanolin, Beeswax, Ozokerite wax, Candelilla wax, Parafin, Aqua (Water), Polysorbate 60, 2-DG, Ethoxydiglycol, Menthol, Tocopheryl, Cholecalciferal, Retinyl Palmitate, Phytonadione

  • Package Labeling:

    Outer

  • INGREDIENTS AND APPEARANCE
    LIPROTEK 
    petrolatum, lidocaine ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67194-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM610 mg  in 1 g
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE6 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    JOJOBA OIL (UNII: 724GKU717M)  
    LANOLIN (UNII: 7EV65EAW6H)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CERESIN (UNII: Q1LS2UJO3A)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    2-DEOXYGLUCOSE (UNII: 9G2MP84A8W)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    MENTHOL (UNII: L7T10EIP3A)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    PHYTONADIONE (UNII: A034SE7857)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67194-017-014 g in 1 JAR; Type 0: Not a Combination Product01/21/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/21/2016
    Labeler - Unit Dose, Ltd. (119080393)
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