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Salicylic Acid Corn Remover

Dosage form: strip
Ingredients: SALICYLIC ACID 40mg
Labeler: ASO Pharmaceutical Co. Ltd.
NDC Code: 51511-514

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.

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

Stop use and ask a doctor if

discomfort last

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions
  • wash affected area
  • may soak in warm water for 5 minutes
  • dry area thoroughly
  • remove medicated pad from backing paper by pulling from center of pad
  • apply
  • repeat after 48 hours remove medicated bandage
  • repeat procedure every 48 hours as needed (until corn is removed) for up to 14 days

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

Inactive ingredients

lanolin, polybutene, rosin ester, rubber

Distributed by:
ASO LLC
Sarasota, FL 34240

*This product is not manufactured or distributed by Schering-Plough
HealthCare Products Inc.

Principal Display Panel
SALICYLIC ACID CORN REMOVER 
salicylic acid strip
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51511-514
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID40 mg
Inactive Ingredients
Ingredient NameStrength
LANOLIN 
NATURAL LATEX RUBBER 
Packaging
#Item CodePackage Description
1NDC:51511-514-011 POUCH in 1 BOX
16 STRIP in 1 POUCH
2NDC:51511-514-062400 POUCH in 1 BOX
26 STRIP in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358B02/01/2010
Labeler - ASO Pharmaceutical Co. Ltd. (690629019)
Establishment
NameAddressID/FEIOperations
ASO LLC152793493REPACK(51511-514)
Establishment
NameAddressID/FEIOperations
Aso Americas, S. de R.L. de C.V.815341862REPACK(51511-514)

Revised: 07/2012
Document Id: 0ce3d56c-6195-4eee-bb7c-d3a9392c96b6
Set id: 66063960-643d-4351-a134-37a0eb4de6ed
Version: 4
Effective Time: 20120703
 
ASO Pharmaceutical Co. Ltd.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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