Label: TATTOO NUMBING CREAM- lidocaine paste

  • NDC Code(s): 84023-201-01
  • Packager: Shenzhen Yangan Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 8, 2024

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  • SPL UNCLASSIFIED SECTION

    Tattoo Numbing Cream

  • ACTIVE INGREDIENT

    Lidocaine 5%

  • PURPOSE

    Topical Anesthetic

  • INDICATIONS & USAGE

    For temporary relief of local discomfort, itching, pain, soreness, or burning in the perianal area associated with anorectal disorders.

  • WARNINGS

    For external use only

  • DO NOT USE

    Pregnant or breastfeeding, ask a health professional before use.

  • WHEN USING

    Do not exceed the recommended daily dosage unless directed by a doctor.
    Do not put into the rectum by using fingers or any medical device or applicator.

  • STOP USE

    Condition worsens, or does not improve within 7 days. Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation,swelling, pain, or other symptoms develop or increase, discontinue use.

  • KEEP OUT OF REACH OF CHILDREN

    In case of accidental ingestion, seek madical attention immediately.

  • DOSAGE & ADMINISTRATION

    Adults and Children 12 years and older: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth, before application of this product. Apply externally to the affected area up to 6 times daily.

  • STORAGE AND HANDLING

    Keep away from direct sunlight or heat.
    Store in room temperature (59-86°F/15-30°C).

  • INACTIVE INGREDIENT

    Aloe barbadebsis leaf juice (Aloe vera)
    Water
    Lecithin (Soybean)
    Propylene Glycol
    Tocopheryl Acetate
    Carbomer
    Menthol
    Triethanolamine

  • PRINCIPAL DISPLAY PANEL

    label4label5

  • INGREDIENTS AND APPEARANCE
    TATTOO NUMBING CREAM 
    lidocaine paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84023-201
    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
    ALOE (UNII: V5VD430YW9)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    MENTHOL (UNII: L7T10EIP3A)  
    WATER (UNII: 059QF0KO0R)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84023-201-011 in 1 BOX01/30/2024
    160 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 DrugM01701/30/2024
    Labeler - Shenzhen Yangan Technology Co., Ltd. (419283765)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Yangan Technology Co., Ltd.419283765manufacture(84023-201)
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