DR. NUMB - lidocaine cream 
Ei Inc.

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.

----------

Dr. Numb Anorectal Cream

Acive Ingredients Purpose

Lidocaine 5% Local Anesthetic

Uses

For temprary relief of local discomfort, itching pain, soreness or burning in the perianal area associated with anorectal disorders.For temprary relief of local discomfort, itching pain, soreness or burning in the perianal area associated with anorectal disorders.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

For temporary relief of local discomfort, itching, pain, soreness or burning in the perianal area assosiated with anorectal disorders.

Warnings

For external use only

When using this product

​Stop use and ask a doctor if

Directions

​Inactive ingredients

Carbopol, lecithin, propylene glycol, purified water, vitamin E.

​Other information

Questions and comments?

Call weekdays 8 a.m. to 5 p.m. PST at 8-877-786-2001 oe email us at support@drnumb.com

Labeling

Tube
Unit Carton
DR. NUMB 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:52512-130
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lidocaine (Lidocaine) Lidocaine5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Propylene Glycol 
Benzyl Alcohol 
.ALPHA.-TOCOPHEROL ACETATE 
LECITHIN, SOYBEAN 
CARBOMER HOMOPOLYMER TYPE B 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52512-130-301 in 1 PACKAGE
130 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34811/15/2012
Labeler - Ei Inc. (105803274)
Registrant - Ei Inc. (105803274)
Establishment
NameAddressID/FEIBusiness Operations
Ei Inc.105803274manufacture(52512-130), label(52512-130), pack(52512-130)

Revised: 12/2012
Document Id: 1ce5f34a-abc9-4ea8-b654-407ecf954440
Set id: 041b4835-bf12-4a36-9fbc-bf253ed805cf
Version: 1
Effective Time: 20121207
 
Ei Inc.