FDA.reportPublic FDA data

Salicylic Acid

Manufacturer
FSA Store Inc.
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:38:18

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the removal of corns and calluses relieves pain by removing corns and calluses

Dosage and administration

wash the affected area and dry thoroughly apply one drop at a time with applicator to sufficiently cover each corn/callus let dry use cushion with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately) hold cushion down 2-3 seconds to adhere to skin repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed) may soak corn/cal...

Label contents#

Full prescribing information#

​Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%w/w

​Purpose

OTC - PURPOSE SECTION

Corn and callus remover

​Uses

INDICATIONS & USAGE SECTION

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

​Warnings

WARNINGS SECTION

​For external use only.

Flammable

SAFE HANDLING WARNING SECTION

  • keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

  • if product gets into the eye, flush with water for 15 minutes
  • avoid inhaling vapors
  • cap bottle tightly and store at room temperatuer away from heat

Stop use and ask a doctor if

OTC - STOP USE SECTION

discomfort persists

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

​Directions

DOSAGE & ADMINISTRATION SECTION

  • wash the affected area and dry thoroughly
  • apply one drop at a time with applicator to sufficiently cover each corn/callus
  • let dry
  • use cushion with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
  • hold cushion down 2-3 seconds to adhere to skin
  • repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
  • may soak corn/callus in warm water for 5 minutes to assist in removal

​Other information

OTHER SAFETY INFORMATION

  • store between 20° - 25°C (68°- to 77°F)
  • avoid surrounding skin when applying product
  • close tightly to prevent solidifciation
  • wipe top of bottle clean after each use
  • do not allow to come into contact with fabrics, floors, countertops or other surfaces- will stain

​Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

​Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

caring mill

Liquid Corn &

Callus Remover

Salicylic Acid 17% / Corn & Callus Remover

Safely removes corns & calluses

Soft foam cushions & protects

0.33 FL.OZ. (9.8 mL) 3 Cushions

cartoncarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312881salicylic acid 17 % Topical SolutionPSN2
312881salicylic acid 170 MG/ML Topical SolutionSCD2
312881salicylic acid 17 % Topical SolutionSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81522-956-01Salicylic Acid9.8 mL in 1 BOTTLE, WITH APPLICATORLIQUID9.82
81522-956-01Salicylic Acid1 in 1 CARTONLIQUID12

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81522-95681522-956-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ETHYL ETHER0F5N573A2YIACT
SALICYLIC ACIDO414PZ4LPZACTIB
CASTOR OILD5340Y2I9GIACT
CAMPHOR (NATURAL)N20HL7Q941IACT
NITROCELLULOSEKYR8BR2X6OIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-08-19full-release2026-06-01 01:11:14

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Salicylic AcidLIQUID CORN AND CALLUS REMOVERFSA Store Inc.3cd18e4c-26c1-1548-e063-6294a90acdb02025-10-08WarningsExact identifier
ndc (package): 81522-956-01
ndc (product): 81522-956
ndc11 (package): 81522095601
spl id: 40ab8905-1df6-698f-e063-6394a90aec4c
spl set id: 3cd18e4c-26c1-1548-e063-6294a90acdb0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.