ADVANCED NUMB TOPICAL ANESTHETIC- lidocaine hydrochloride cream 
Uber Scientific, LLC

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ADVANCED NUMB Topical Anesthetic

DRUG FACTS

Active Ingredients

Lidocaine HCL (5%)

Purpose

External Analgesic

Use

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

Warnings

For external use 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

Adults and children 12 years and older:  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.

Apply externally up to 6 times per day.

Children under 12: Consult a Doctor.

Inactive ingredients

Allantoin Gel, Deionized Water, Benzyl Alcohol, Carbomer, Pro-pylene GLycol, Sodim Polyacrylate, Tocopheryl Acetate (Vitamin E), Triethanolamine

Other Information

Store at room temperature. Avoid Direct sunlight.

Package Labeling:

Jar

ADVANCED NUMB TOPICAL ANESTHETIC 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71131-052
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 (UNII: H4N855PNZ1)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71131-052-0257 g in 1 JAR; Type 0: Not a Combination Product04/20/201812/31/2020
2NDC:71131-052-04114 g in 1 JAR; Type 0: Not a Combination Product04/20/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01504/20/2018
Labeler - Uber Scientific, LLC (080459429)

Revised: 10/2023
Document Id: 07986186-7a16-cd1e-e063-6394a90a5e7e
Set id: 859d1cad-badf-4c42-9b08-daacb3fae8b4
Version: 10
Effective Time: 20231013
 
Uber Scientific, LLC