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.

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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 Type HUMAN OTC DRUG Item Code (Source) NDC:52512-130
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Lidocaine (UNII: 98PI200987) (Lidocaine - UNII:98PI200987) Lidocaine 5 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
Propylene Glycol (UNII: 6DC9Q167V3)  
Benzyl Alcohol (UNII: LKG8494WBH)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52512-130-30 1 in 1 PACKAGE
1 30 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part348 11/15/2012
Labeler - Ei Inc. (105803274)
Registrant - Ei Inc. (105803274)
Establishment
Name Address ID/FEI Business Operations
Ei Inc. 105803274 manufacture(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.