One Step Corn Removers (Scapa)

Scholls Wellness Company LLC by

Drug Labeling and Warnings

Scholls Wellness Company LLC by is a Otc medication manufactured, distributed, or labeled by Scapa Tapes North America LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SCHOLLS WELLNESS COMPANY LLC ONE STEP CORN REMOVERS- salicylic acid disc 
Scapa Tapes North America LLC

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 Removers (Scapa)

Drug Facts

Drug Facts

Active Ingredient

Active Ingredient Purpose

Salicylic Acid 40%.......................Corn remover

Purpose

Corn remover

Uses

Uses

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

Warnings

Warnings

For external use only

Do not use

Do not use

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

Stop use and ask a doctor

Stop use and ask a doctor if discomfort lasts

Keep out of reach of children

Keep out of reach of children​. If swallowed,

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

Directions

Directions​

  • wash affected area and dry thoroughly
  • apply medicated bandage
  • after 48 hours, remove medicated bandage
  • 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 removal

Other information

Other information​

  • store between 20ºC to 25ºC (68º to 77ºF).
  • Protect from excessive heat (temperatures above 40ºC (104ºF))

Inactive ingredients

Inactive ingredients​ antioxidant

(CAS 991-84-4), iron oxides, mineral oil,

petroleum hydrocarbon resin, silicon dioxide,

synthetic polyisoprene rubber, talc

Questions

Questions​? 1-866-360-3226

One Step Corn Remover-6CT

SCHOLLS WELLNESS COMPANY LLC  ONE STEP CORN REMOVERS
salicylic acid disc
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66843-075
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.4 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MINERAL OIL (UNII: T5L8T28FGP)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorbrownScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 66843-075-316 in 1 CARTON01/01/2021
11 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F01/01/2021
Labeler - Scapa Tapes North America LLC (079995435)
Registrant - Scapa Tapes North America LLC (079995435)

Revised: 1/2022