Label: DERMA NUMB- lidocaine hydrochloride spray 

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

Drug Label Information

Updated 10/12

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

  • Active Ingredients

    Lidocaine HCI

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  • Purpose

    Topical Anesthetic

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  • Uses

    Temporarily relieves pain from tattoo procedures.

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  • Directions

    First test product to sensitivity to skin.

    Once skin is broken or outline is done, apply derma numb generously to tattooed area.

    Wait two minutes for anesthetic to take affect, re-apply derma numb to tattoo area as needed through out the tattoo process for comfort. Discontinue use if sensitivity occurs. Do not use on face.

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  • Warnings

    External Use Only

    Avoid contact with the eyes

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  • Do Not Use

    If you have any known allergy or sensitivity to any of these ingredients in this product. Discontinue use and seek medical attention.

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  • Stop Use and ask a doctor if

    • skin becomes irritated • condition worsens or symptoms last more than7 days • symptoms clear up and reoccur with a few days

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  • Inactive ingredients

    Water, Propylene Glycol, Achillea Millefolium (Yarrow) Extract, Yucca Glauca Root Extract, Citric Acid, Sodium Metabisulfate, Caprylyl Glycol, Disodium EDTA, Methylisothiazolinone.

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  • Other Information

    This product was manufactured for Atlas Tat, Inc.

    Any questions call 954-492-9898 or check out the web @ dermnumb.com

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  • INGREDIENTS AND APPEARANCE
    DERMA NUMB 
    lidocaine hci spray
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:53200-001
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE 40 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM METABISULFITE  
    PROPYLENE GLYCOL  
    EDETATE DISODIUM  
    ACHILLEA MILLEFOLIUM  
    YUCCA GLAUCA ROOT  
    DIAZOLIDINYL UREA  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:53200-001-01 28.35 g in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part348 07/15/2012
    Labeler - Atlas Tat Inc. (061275633)
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