MOSCO- 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.

----------

Mosco

MOSCO LIQUID CALLUS & CORN REMOVER

Drug Facts

Active ingredient

Salicylic Acid 17.6%

Purpose

Callus & corn remover

Use

For removal of calluses and corns

Warnings

For external use only

  • Extremely flammable
  • Keep away from fire or flame. Avoid smoking during use and until product has dried.
  • Cap bottle tightly after each use and store at room temperature away from heat.
  • Avoid inhaling vapors.
  • If product gets into the eye, flush with water for 15 minutes.

Do not use:

  • on irritated skin
  • on any area that is reddened or infected

Ask a doctor before use if you have:

  • diabetes
  • poor blood circulation
  • if you have diabetes or poor blood circulation

Stop use and ask a doctor

if discomfort persists

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

Other information

  • Store at room temperature
  • Avoid excessive heat

Inactive ingredients

alcohol, ether

Questions?

1-800-443-4908

PRINCIPAL DISPLAY PANEL

MOSCO LIQUID
CALLUS
& CORN
REMOVER

PRINCIPAL DISPLAY PANEL MOSCO LIQUID CALLUS & CORN REMOVER

MOSCO 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-309
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID150 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ETHER (UNII: 0F5N573A2Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-309-031 in 1 CARTON10/01/199905/31/2022
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 finalpart358F10/01/199905/31/2022
Labeler - Medtech Products Inc. (122715688)

Revised: 3/2023
Document Id: 2a2a4102-9400-43c1-a252-e9f2bd47a008
Set id: a862bd50-e160-43f0-87fb-e388d05f5537
Version: 2
Effective Time: 20230313
 
Medtech Products Inc.