Label: UBER NUMB- lidocaine hydrochloride cream

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

Drug Label Information

Updated November 10, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active Ingredients

    Lidocaine HCL (5%)

    Purpose

    External Analgesic

  • Uses

    For the Temporary relief of pain and discomfort associated with anorectal disorders

  • Warnings:

    For external ues only. If condition worsens or does not improve within 7 days, consult a doctor. Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, consult a doctor promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator. 

    Keep out of reach of children.

    If swallowed, get medical help or contact the Poison Control Center immediately

  • Directions:

     For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly, Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product. Adults and children 12 years and older:

    Apply externally up to 6 times per day.

    Consult a Doctor Children under 12: 

  • Inactive Ingredients:

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

  • Distributed by:

    UberScientific LLC 838 E High St. Ste 271

    Lexington, KY 40502

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    UBER NUMB 
    lidocaine hydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71131-051
    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
    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:71131-051-021 in 1 CARTON11/01/2017
    157 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/01/2017
    Labeler - UBERScientific, LLC (080459429)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!