CORN REMOVERS- salicylic acid plaster 
Cuxson Gerrard & 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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CARNATION CORN REMOVERS

Active ingredient

Salicylic acid 40% w/w

Purpose

Corn remover

Uses

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

Warnings

For External Use Only

Do not use

  • Contains Peanut Oil. Do not use if you are allergic to peanut or soya.
  • 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 or podiatrist if

discomfort persists

Keep out of reach and sight of children.

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

Directions

  • clean and dry the affected area
  • remove a corn plaster from the backing film and position the felt ring over the corn
  • firmly apply in position with adhesive strap
  • when properly applied it should not slip or move
  • remove the plaster after 48 hours
  • repeat procedure every 48 hours as needed (until corn is removed) for up to 10 days

Other information

store at room temperature

avoid excessive heat (30ºC, 86ºF)

Inactive ingredients

partially hydrogenated wood rosin, peanut oil, ponceau 4R, rubber based adhesive , sunset yellow, vegetable triglyceride, yellow beeswax

Product Type

Human OTC Drug Label

Route of Administration

Topical

Packaging

5 plasters per carton

30 cartons per display case

Manufactured by:
Cuxson Gerrard & Co Ltd
West Midlands, England B69 4BF

Principal Display Panel - Carton Label

CARNATION ®

FOOTCARE

MAXIMUM STRENGTH • ONE-STEP

Corn Removers

salicylic acid

Active
medicated
center

Self-
adhesive
plaster

Felt
pad relieves
pressure

5 MEDICATED PLASTERS

Principal Display Panel - Carton Label
CORN REMOVERS 
salicylic acid plaster
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61447-001
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
ROSIN (UNII: 88S87KL877)  
PEANUT OIL (UNII: 5TL50QU0W4)  
PONCEAU 4R (UNII: Z525CBK9PG)  
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
C10-18 TRIGLYCERIDES (UNII: 43AGM4PHPI)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61447-001-0530 in 1 CASE03/01/201407/21/2017
15 in 1 CARTON; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H03/01/201407/21/2017
Labeler - Cuxson Gerrard & Co Ltd (218908218)

Revised: 8/2017
Document Id: 55dc40db-0c65-04ff-e054-00144ff88e88
Set id: 29fed517-1e1f-4b3a-a7c0-9def6dbbd734
Version: 2
Effective Time: 20170803
 
Cuxson Gerrard & Co Ltd