Label: ATOZCUP TATTOO NUMBING- lidocaine cream

  • NDC Code(s): 83706-001-02
  • Packager: Dongguan City Bobiter Electronic Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2023

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  • Active Ingredient(s)

    Lidocaine 5%

  • Purpose

    local anesthetic

  • Use

    For temporary relief of local discomfort, itching, pain,soreness or burning of the skin

  • Warnings

    For external use only.

  • Do not use

    Do not exceed the recommended daily dosage unless directed by a doctor.

  • WHEN USING

    When using Avoid contact with eyes. If this happens, rinse thoroughly with water.

  • STOP USE

    lf allergy occurs such as redness,irritation,swelling,pain or other symptoms become severe Stop use and get to a doctor.If symptoms persist for more than 7days or subside but occur again within3 days,stop use and consult aphysician.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. 

  • Directions

    1.Wash and exfoliate the area to be treated.
    2.Dry the area completely.

    3.Apply this numbing cream(2mm thick) to the area and rub in thoroughly

    4.Cover with cling film.

    5.leave the cream and wrap in place for 60-90 minutes before procedure.

    6.After the wrapping time,remove thecling film and wipe the cream away

  • Storage and handling

    *Always keep tihgtly closed

    *Store at temperatures between 59°F-86°F(15°C-30°C)

    *Protectfrom freezing

  • Inactive ingredients

    Lecithin(Soybean)，Propylene Glycol，Tocopheryl Acctate,Aloe Vera，Water，Carbomer,Menthol，Triethanolamine

  • Package Label - Principal Display Panel

    image description

  • INGREDIENTS AND APPEARANCE
    ATOZCUP TATTOO NUMBING 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83706-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83706-001-021 in 1 PACKAGE09/22/2023
    130 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01709/22/2023
    Labeler - Dongguan City Bobiter Electronic Technology Co., Ltd (411899304)
    Registrant - Dongguan City Bobiter Electronic Technology Co., Ltd (411899304)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dongguan City Bobiter Electronic Technology Co., Ltd411899304manufacture(83706-001)
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