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Uber Numb Topical Anesthetic by UberScientific, LLC

Medically reviewed on December 20, 2016

Dosage form: cream
Ingredients: LIDOCAINE HYDROCHLORIDE 50mg in 1g
Labeler: UberScientific, LLC
NDC Code: 71131-774

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Uber Numb Topical Anesthetic Cream

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:
  • Adults and children 12-years and over: apply to affected area.
  • Children under 12, consult a physician before use.
  • 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:

UBER NUMB TOPICAL ANESTHETIC 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71131-774
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN 
WATER 
BENZYL ALCOHOL 
CARBOXYPOLYMETHYLENE 
PROPYLENE GLYCOL 
.ALPHA.-TOCOPHEROL ACETATE 
TROLAMINE 
Packaging
#Item CodePackage Description
1NDC:71131-774-0128.35 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34612/20/2016
Labeler - UberScientific, LLC (080459429)

 
UberScientific, LLC

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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