ASPER FLEX- lidocaine cream 
Akron Pharma Inc.

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Asper Flex (Lidocaine 4% Cream)

Topical Anesthetic Cream

FOR EXTERNAL USE ONLY

Active ingredient

Lidocaine 4% w/w

Purpose

Topical anesthetic

Uses

temporarily relieves pain and itching due to

Warnings

For external use only

Do not use

Directions

For external use only

Do not use

  • in or near the eyes
  • in large quantities, particularly over raw or blistered areas

Stop use and ask a doctor if

  • allergic reaction occurs
  • condition worsens or does not improve within 7 days
  • symptoms clear up and return within a few days
  • redness, irritation, swelling, pain or other symptoms begin or increase

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other information

Inactive ingredients

Benzyl Alcohol, Carbopol 940, Hydrogenated Lecithin, Polysorbate 80, Propylene Glycol, Puried Water, Trolamine and Vitamin E Acetate.

Questions or comments?

Call toll-free 1-877-255-6999

Manufactured for:

Akron Pharma Inc.

Fairfield, Nj 07004

www.akronpharma.com

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ASPER FLEX 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71399-0049
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
Product Characteristics
Colorwhite (clear gel) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71399-0049-51 in 1 CARTON11/03/2023
15 g in 1 PACKAGE; Type 0: Not a Combination Product
2NDC:71399-0049-11 in 1 CARTON11/03/2023
215 g in 1 PACKAGE; Type 0: Not a Combination Product
3NDC:71399-0049-31 in 1 CARTON11/03/2023
330 g in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/03/2023
Labeler - Akron Pharma Inc. (067878881)

Revised: 4/2023
Document Id: 640a4f75-dcd4-438f-9859-2d0b476b86a0
Set id: 06ddae64-cda7-4eb9-872f-5182c83cb00c
Version: 1
Effective Time: 20230403
 
Akron Pharma Inc.