DR. NUMB- lidocaine cream 
Shinpharma Inc

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Drug Facts

Active ingredient

Lidocaine 5%

Purpose

Anorectal (Hemmorhoidal)

Uses

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

Warnings

For external use only

When using this product

  • do not exceed the recommended daily dosage unless directed by a doctor
  • do not put into the rectum by using fingers or any mechanical device or applicator

Stop the use and consult doctor if

  • allergic reaction occurs
  • rectal bleeding occurs
  • redness, irritation, swelling, pain, or other symptoms begin or increase
  • condition worsens or does not improve within 7 days

keep out of reach of children

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

Directions

Other information

Inactive Ingredients

Benzyl Alcohol, Carbopol, Lecithin, Propylene Glycol, Tocopheryl Acetate, Water.

Question or comments

Contact our dedicated Customer Care at 1-877-786-2001 or email us at support@shinpharma.com 

Principal Display Panel

NDC 69903-001-30

Prompt, Soothing Relief from Painful Burning, Itching and Discomfort

5% Lidocaine Cream

For External Use Only

Dr. Numb Lidocaine Cream

RAPID ABSORPTION

Maximum Strength Pain Reliever

30g

Label

DR. NUMB 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69903-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE1.5 g  in 30 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
PROPYLENE GLYCOL BUTYL ETHER (UNII: 6X8776AP5Z)  
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69903-001-301 in 1 CARTON07/01/2016
130 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01507/01/2016
Labeler - Shinpharma Inc (248552403)
Registrant - Shinpharma Inc (248552403)

Revised: 4/2024
Document Id: 153a2ee5-e753-9e39-e063-6394a90acedd
Set id: 32ab24b4-dcec-4a09-e054-00144ff88e88
Version: 7
Effective Time: 20240403
 
Shinpharma Inc