SALICYLIC ACID CORN 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 Corn Remover Strips

Maximum Strength

Active ingredient

Salicylic acid 40%

Purpose

Corn remover

Uses

  • for the removal of corns.
  • relieves pain by removing corns

Warnings

For External Use Only

Do not use

  • on irritated skin
  • on any area that is infected or reddened
  • if you have poor blood circulation
  • if you are diabetic

Stop use and ask a doctor if

discomfort lasts

Keep out of reach of children.

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

Directions

  • Wash affected area and dry thoroughly
  • Remove medicated pad from backing paper by pulling from center of pad
  • Apply
  • After 48 hours, remove medicated pad
  • Repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
  • May soak corn in warm water for 5 minutes to assist in removal

Other information

  • store at room temperature
  • avoid excessive heat 99ºF (37ºC)

Inactive ingredients

lanolin, polybutene, rosin ester, rubber

Distributed by:

ASO LLC
Sarasota, FL 34240

Made in Japan

*This product is not manufactured or distributed by he Bayer Corporation, owners of the registered trademark Dr. Scholl’s®.

Principal Display Panel

ONE STEP

CORN REMOVER

MAXIMUM STRENGTH

SALICYLIC ACID 40%

  • Cushions & helps relieve pain
  • Convenient 1-step bandage
  • Waterproof

Front Panel Corn Remover

SALICYLIC ACID CORN REMOVER 
salicylic acid strip
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51511-514
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:51511-514-011 in 1 BOX02/01/201002/28/2022
16 in 1 POUCH; Type 0: Not a Combination Product
2NDC:51511-514-242400 in 1 CARTON02/01/201002/28/2022
2200 in 1 TRAY
26 in 1 POUCH; Type 0: Not a Combination Product
3NDC:51511-514-181800 in 1 CARTON01/08/201009/30/2021
3150 in 1 TRAY
38 in 1 POUCH; Type 0: Not a Combination Product
4NDC:51511-514-081 in 1 BOX01/08/201009/30/2021
48 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM03001/08/201002/28/2022
Labeler - ASO Pharmaceutical Co. Ltd. (690629019)

Revised: 7/2022
Document Id: e4df1cb1-c01a-286b-e053-2a95a90a97b6
Set id: 66063960-643d-4351-a134-37a0eb4de6ed
Version: 7
Effective Time: 20220728
 
ASO Pharmaceutical Co. Ltd.