Label: LORENZA PAIN RELIEF PATCH patch

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 5, 2014

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  • GENERAL PRECAUTIONS

    This product may cause allergic reactions in some individuals.

  • DRUG FACTS

    DrugFacts.jpg

  • DESCRIPTION

    LorenzaBox.jpg

  • INGREDIENTS AND APPEARANCE
    LORENZA PAIN RELIEF PATCH 
    lorenza pain relief patch patch
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69379-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Lidocaine (UNII: 98PI200987) (Lidocaine - UNII:98PI200987) Lidocaine4 g  in 100 g
    Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) Menthol1 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69379-014-175 in 1 BOX01/01/2015
    13 in 1 PACKAGE
    1100 g in 1 PATCH; Type 3: Prefilled Biologic Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2015
    Labeler - Home Aide Diagnostics, Inc. (783518983)