SALICYLIC ACID CORN REMOVERS- salicylic acid strip 
CVS Pharmacy

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
  • May soak in warm water for 5 minutes to assist in removal
  • Dry area thoroughly
  • Remove medicated pad from backing paper by pulling from center of pad
  • Apply
  • Remove pad after 48 hours
  • 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

Principal Display Panel

CVS

Health

Compare to the active ingredient

in Dr. Scholl’s ®*

Maximum Strength

One Step

Medicated

Corn

Removers

SALICYCLIC ACID 40%

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

Actual Size

6 MEDICATED BANDAGES

Label

SALICYLIC ACID CORN REMOVERS 
salicylic acid strip
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-514
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)  
POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)  
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-514-011 in 1 BOX01/01/2016
16 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358B01/01/201602/28/2022
Labeler - CVS Pharmacy (062312574)

Revised: 4/2019
 
CVS Pharmacy