Label: UBER NUMB- lidocaine hydrochloride liquid

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

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active Ingredients

    Lidocaine HCL 5%

    Purpose

    Topical Anesthetic

  • Uses

    Temporarily relieves pain, itching or swelling associated with anorectal disorders. External Use Only.

  • Warnings:

    Keep out of reach of children.

    Do not use if pregnant or breast feeding. For external use only, if accidentally ingested, seek meical attention immediately. Do not use in large quantities, particularly over raw surfaces or blistered areas. Avoid contact with the eyes, if contact with the eyes occur, rinse with copious amounts of eyewash and seek medical attention immediately. Use on small area of skin to test for sensitivities prior to use.

    Do not Use if:

    • you have a history of seizures.
    • you have been diagnosed with liver disease.
    • you have an allergy to any of the ingredients listed. If a reaction or sensitivity occurs, discontinue use and seek medical attention immediately. If condition worsens or symptoms are persistent for more than five days, or recur after clearing up, consult with a medical professional immediately.
  • Directions:

    Prior to using therapeutically, test on small area of skin for sensitivities and possible allergies, if adverse reaction occurs seek medical attention. Spray UberNumb anesthetic spray, sparingly, on affected area. The Area should begin to feel numbing anestehetic relief within two minutes. For continued numbing releif, reapply UberNumb sparingly as needed. If at any point, irritations or other sensitivities occur, discontinue use and seek medical attention Store in a cool dark place or refrigerate. Discard after expiration date

  • Inactive Ingredients:

    Purified Water, Propylene Glycol, Sodium Metabisulfite, Citric Acid, Epinephrine HCL, Diazolidinyl Urea, Methyl Paraben, Propyl Paraben, and Disodium EDTA.

  • Distributed by:

    UberScientific TM 838 E High St. Ste 271 Lexington, KY 40502 302 566 -8237


  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    UBER NUMB 
    lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71131-050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EPINEPHRINE HYDROCHLORIDE (UNII: WBB047OO38)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71131-050-04118.29 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/01/2017
    Labeler - UBERScientific, LLC (080459429)
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