UBER NUMB- lidocaine hydrochloride liquid

Uber Numb by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts

Active Ingredients

Lidocaine HCL 5%

Purpose

Topical Anesthetic

Uses

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

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:

INGREDIENTS AND APPEARANCE

UBER NUMB 
lidocaine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71131-050
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71131-050-04	118.29 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/01/2017

Labeler - UBERScientific, LLC (080459429)

Establishment
Name	Address	ID/FEI	Business Operations
PURE SOURCE, LLC		080354456	manufacture(71131-050)