FREEZONE- salicylic acid liquid 
Medtech Products Inc.

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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Freezone® Liquid Corn & Callus Remover

Drug Facts

Active Ingredient

Salicylic acid 17.6% in a flexible collodion base

Purpose

Corn/Callus Remover

Use

For the removal of corns and calluses

Warnings

For external use only.

  • Extremely flammable. Keep away from fire or flame.
  • Cap bottle tightly and store at room temperature away from heat.

Do not use this product

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

Stop use and ask a doctor if

discomfort persists

When using this product

  • avoid inhaling vapors
  • avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

  • Wash affected area.
  • You may soak callus or corn in warm water for 5 minutes.
  • Dry area thoroughly
  • Apply one drop at a time to cover each corn or callus.
  • Let dry.
  • Repeat procedure once or twice daily as needed for up to 14 days (until corn or callus is removed).

Inactive Ingredients

alcohol 27%, ether 57%

Questions?

1-800-443-4908

Freezone® Liquid Corn & Callus Remover, 0.3 fl oz (9 mL)

Freezone Liquid Corn and Callus Remover Carton
FREEZONE 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-104
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID158.4 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ETHER (UNII: 0F5N573A2Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-104-031 in 1 BOX10/01/1999
19 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F10/01/199906/15/2022
Labeler - Medtech Products Inc. (122715688)

Revised: 3/2023
Document Id: 915b7181-c69a-4bc5-8716-ac511129846f
Set id: f55b64b3-d87d-4c96-9a73-96325059e6b8
Version: 3
Effective Time: 20230303
 
Medtech Products Inc.