Label: UBER NUMB TOPICAL ANESTHETIC- lidocaine hydrochloride cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • DRUG FACTS:

  • Active Ingredient:

    Lidocaine HCl 5.00% 

    Local Anesthetic

  • Uses:

    For the temporary relief of local pain and discomfort associated with anorectal disorders.

  • Warnings:

    • For external use only. Use only as directed.

    When using this product, 

    • do not exceed the recommended daily dosage unless directed by a doctor.
    • Do not insert this product into rectum using fingers or any mechanical device.

    Keep out of reach of children.

    • Children under 12 should consult physician  prior to use.

    Stop using this product if:

    • Symptoms worsen or does not improve within seven days
    • Bleeding occurs. *Redness, irritation, swelling, pain or other symptoms develop.
  • Directions:

    • Apply to affected area. Adults and children 12-years and over:
    •  consult a physician before use. Children under 12,
    • Clean affected area with warm water and mild soap. Rinse thoroughly.
    • Gently dry by patting with toilet tissue or soft cloth.
    • Apply externally to area up to six times per day.

    How to Apply:

  • Other Ingredients:

    Allantoin, Aqua (Deionized Water), Benzyl Alcohol, Carbomer, Propylene Glycol, Sodium Polyacrylate, Tocopheryl Acetate (Vitamin E), Triethanolamine.

  • SPL UNCLASSIFIED SECTION

    Store at room temperature. Avoid direct sunlight

  • Package Labeling:

    Label7

  • INGREDIENTS AND APPEARANCE
    UBER NUMB TOPICAL ANESTHETIC 
    lidocaine hydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71131-797
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    WATER (UNII: 059QF0KO0R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71131-797-04118 mL in 1 JAR; Type 0: Not a Combination Product02/23/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01502/23/2017
    Labeler - UberScientific, LLC (080459429)
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