UBER NUMB TOPICAL ANESTHETIC- lidocaine hydrochloride cream

Uber Numb Topical Anesthetic by

Drug Labeling and Warnings

Uber Numb Topical Anesthetic by is a Otc medication manufactured, distributed, or labeled by UberScientific, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS:

Active Ingredient:

Lidocaine HCl 5.00% 

External analgesic

Uses:

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.

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.

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

Keep out of reach of children.

• Keep out of reach of children.

Directions:

Children under 12, consult a doctor

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.

Other Ingredients:

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

Other Information

Store at room temperature. Avoid Direct Sunlight. Do not use if
tamper evident packaging has been breached or is missing.

Distributed by:

UberScientific LLC
838 E High St - Ste 271
Lexington, KY 40502

Package Labeling:

INGREDIENTS AND APPEARANCE

UBER NUMB TOPICAL ANESTHETIC 
lidocaine hydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71131-797
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71131-797-04	118 mL in 1 JAR; Type 0: Not a Combination Product	02/23/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	02/23/2017

Labeler - UberScientific, LLC (080459429)

Registrant - UberScientific, LLC (080459429)