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,
    • How to Apply:
    • Clean affected area with warm water nad mild soap. Rinse thoroughly.
    • Gently dry by patting with toilet tissue or soft cloth.
    • Apply externally to area up to six times per day.
  • Other Ingredients:

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

    • Store at room temperature. Avoid direct sunlight
  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    UBER NUMB TOPICAL ANESTHETIC 
    lidocaine hydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71131-774
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 g
    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)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71131-774-0128.35 g in 1 JAR; Type 0: Not a Combination Product12/20/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01512/20/2016
    Labeler - UberScientific, LLC (080459429)
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