Label: MAGIC PLUS ANESTHETIC- lidocaine hydrochloride, tetracaine hydrochloride, and racepinephrine hydrochloride liquid

  • NDC Code(s): 84055-008-01
  • Packager: Permanent Make Up Products LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 11, 2024

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  • ACTIVE INGREDIENTS

    5.00% LIDOCAINE HYDROCHLORIDE, 2.00% TETRACAINE HYDROCHLORIDE, 0.02% RACEPINEPHRINE HYDROCHLORIDE

  • INACTIVE INGREDIENTS

    DEIONIZED WATER, SODIUM METABISULFITE, SODIUM CHLORIDE, PROPYLENE GLYCOL, METHYLPARABEN, PROPYLPARABEN, DIAZOLIDINYL UREA, AND TETRASODIUM EDTA

  • FOR EXTERNAL USE ONLY

    For temporary relief of pain and swelling.

  • DIRECTIONS

    Sensitivity test is strongly advised prior to use. Apply to area for temporary relief. Do not use more than 2 times a day.

  • STORAGE AND HANDLING

    Store in a cool, dark place. Do not refrigerate.

  • WARNINGS

    CLIENT EYE PROTECTANT SUGGESTED

    Do not get in the mouth or eyes. Do not use product if you are pregnant or a nursing mother.

    Keep out of the reach of children. If product comes into contact with the eyes wash immediatley. If accidentally swallowed seek immediate medical attention.

    Do not use this product if you have any allergies to any of the product ingredients.

    CAUTION

    DISCONTINUE USE IF YOU HAVE SKIN IRRITATION OR SENSITIVITY.

  • SPL UNCLASSIFIED SECTION

    Distributed by
    Permanent Make Up Products LLC.

  • PRINCIPAL DISPLAY PANEL - 28 G Bottle Label

    MAGIC
    PLUS TOPICAL ANESTHETIC SPRAY

    SPRAY!

    RELIEVES PAIN & SWELLING
    WORKS IN SECONDS
    FOR PROFESSIONAL USE ONLY

    1 FL OZ. (28G)

    PERMANENTMAKEUPPRODUCTS.COM 800.984.4331

    PRINCIPAL DISPLAY PANEL - 28 G Bottle Label
  • INGREDIENTS AND APPEARANCE
    MAGIC PLUS ANESTHETIC 
    lidocaine hydrochloride, tetracaine hydrochloride, and racepinephrine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84055-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Lidocaine Hydrochloride (UNII: V13007Z41A) (Lidocaine - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS50 g  in 1000 g
    Tetracaine Hydrochloride (UNII: 5NF5D4OPCI) (Tetracaine - UNII:0619F35CGV) Tetracaine Hydrochloride20 g  in 1000 g
    Racepinephrine Hydrochloride (UNII: 336096P2WE) (Racepinephrine - UNII:GR0L9S3J0F) Racepinephrine200 mg  in 1000 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Water (UNII: 059QF0KO0R)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Propylparaben (UNII: Z8IX2SC1OH)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Diazolidinyl Urea (UNII: H5RIZ3MPW4)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84055-008-011 in 1 BOX04/01/2024
    128 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM01704/01/2024
    Labeler - Permanent Make Up Products LLC. (030421491)
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