SALICYLIC ACID- corn and callus remover liquid 
Chain Drug Consortium, LLC

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Premier Value Liquid Corn And Callus Remover

​Active ingredient

Salicylic acid 17%w/w

Purpose

Corn and callus remover

Uses

​Warnings

Flammable

  • keep away from fire or flame
  • cap bottle tightly and store at room temperature away heat

Do not use

  • on irritated skin
  • on any area that is infected or reddened
  • if you are a diabetic, or if you have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

When using this product

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

Stop and ask a doctor if

discomfort persists, see your doctor or podiatrist

Keep out of reach of children.

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

​Directions

Other information

store between 20°C to 30°C (68°F to 86°F)

Inactive ingredients

camphor, castro oil, ethanol, ethyl ether, nitrocellulose

Questions?

Call 1-866-964-0939

​Principal Display Panel

Premier Value

Liquid Corn And Callus Remover

with Salicylic Acid

3 Cushions

1/3 FL OZ (9.8 mL)

Premier Value Liquid Corn and Callus Remover Card

SALICYLIC ACID 
corn and callus remover liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-610
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.17 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
PYROXYLIN (UNII: KYR8BR2X6O)  
CASTOR OIL (UNII: D5340Y2I9G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-610-0015 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product05/23/200312/13/2017
2NDC:68016-610-099.8 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product05/23/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03005/23/2003
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 2/2024
Document Id: 106a7c03-1ed4-89c0-e063-6294a90a3113
Set id: cbd07fb2-587c-4c0c-b4a9-3b49c22cc562
Version: 9
Effective Time: 20240202
 
Chain Drug Consortium, LLC