SALICYLIC ACID WART REMOVER- salicylic acid strip 
ASO Pharmaceutical Co. Ltd.

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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One Step Wart Remover Strips

Maximum Strength

Active ingredient

Salicylic acid 40%

Purpose

Wart remover

Uses

Warnings

For External Use Only

Do not use

  • on irritated skin or on any area that is infected or reddened
  • on moles, birthmarks, warts with hair growing from them, genital warts, or on warts on the face or mucous membranes
  • if you are diabetic
  • if you have poor blood circulation

Stop use and ask a doctor if you have

discomfort persists

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Other information

Inactive ingredients

lanolin, polybutene, rosin ester, rubber

Distributed by:
ASO LLC
Sarasota, FL 34240

*This product is not manufactured or distributed by Medtech Products, Inc.,
owners of the registered trademark, Compound W®.

Principal Display Panel - Carton (Clear)

ONE STEP

WART REMOVER

MAXIMUM STRENGTH

EFFECTIVELY REMOVES WARTS

SHAPE OF THE PAD HIFES THE WART

Front Panel Clear Wart Remover

Principal Display Panel - Carton (Tan)

ONE STEP

WART REMOVER

MAXIMUM STRENGTH

EFFECTIVELY REMOVES WARTS

SHAPE OF THE PAD HIFES THE WART

Front Panel Tan Wart Remover

SALICYLIC ACID WART REMOVER 
salicylic acid strip
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51511-596
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg
Inactive Ingredients
Ingredient NameStrength
LANOLIN (UNII: 7EV65EAW6H)  
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51511-596-011 in 1 BOX02/01/2009
114 in 1 POUCH; Type 0: Not a Combination Product
2NDC:51511-596-121200 in 1 CARTON02/01/2009
2100 in 1 TRAY
214 in 1 POUCH; Type 0: Not a Combination Product
3NDC:51511-596-101 in 1 BOX10/06/2017
310 in 1 POUCH; Type 0: Not a Combination Product
4NDC:51511-596-141440 in 1 CARTON10/06/2017
4120 in 1 TRAY
410 in 1 POUCH; Type 0: Not a Combination Product
5NDC:51511-596-202 in 1 BOX03/15/2014
510 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H02/01/2009
Labeler - ASO Pharmaceutical Co. Ltd. (690629019)

Revised: 5/2022
Document Id: de5c73a8-a549-36e7-e053-2a95a90a357f
Set id: 6f2bbdee-4c68-4138-b52f-c0e4534e7985
Version: 7
Effective Time: 20220506
 
ASO Pharmaceutical Co. Ltd.