Equate One Step Corn Remover Pad

Dosage form: liquid
Ingredients: SALICYLIC ACID 40mg
Labeler: Wal-Mart Stores Inc.
NDC Code: 49035-152

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 Pad

Drug Facts

Active ingredient

Salicylic Acid 40%

Purpose

Corn Remover

Use

For the removal of corns

Warnings

For external use only

Do not use
  • on irritated skin
  • on any area that is infected or reddened
  • if you are a diabetic
  • if you have poor blood circulation

When using this product

if discomfort persists, see your doctor or podiatrist

Keep out of reach of children.

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

Directions
  • wash affected area
  • may soak corn in warm water for 5 minutes to soften
  • dry area thoroughly
  • remove medicated pad from backing paper by pulling from center of pad
  • apply
  • 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

Inactive ingredients

lanolin, polybutene, rosin ester, rubber

Questions?

Call: 1-888-287-1915

PRINCIPAL DISPLAY PANEL

Maximum Strength
One Step Corn Remover Pads
Salicylic Acid
6 Medicated Pads

EQUATE ONE STEP CORN REMOVER PAD 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-152
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID40 mg
Inactive Ingredients
Ingredient NameStrength
LANOLIN 
ROSIN 
Product Characteristics
ColorPINKScore    
ShapeROUNDSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:49035-152-016 BAG (6 PATCH) in 1 BOX
11 LIQUID (1 PATCH) in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart358B10/01/2010
Labeler - Wal-Mart Stores Inc. (051957769)
Establishment
NameAddressID/FEIOperations
Aso Americas S.690629019MANUFACTURE

Revised: 10/2010
 
Wal-Mart Stores Inc.

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 combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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