Salicylic Acid

Manufacturer
HEB
Effective date
2026-01-15
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:33:13

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

for the removal of corns relieves pain by removing corns

Dosage and administration

wash affected area and dry area thoroughly if necessary, cut medicated patch to fit corn apply adhesive side down of medicated patch onto corn cover medicated patch with pad after 48 hours, remove medicated patch repeat procedure every 48 hours as needed for up to 14 days (until corn is removed) may soak corn in warm water for 5 minutes to assist in removal

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

​Purpose

OTC - PURPOSE SECTION

Corn Remover

​Uses

INDICATIONS & USAGE SECTION

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

​Warnings

WARNINGS SECTION

​For external use only.

​Do not use

OTC - DO NOT USE SECTION

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

Stop Use and ​Ask a doctor 

OTC - STOP USE SECTION

if 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 affected area and dry area thoroughly
  • if necessary, cut medicated patch to fit corn
  • apply adhesive side down of medicated patch onto corn
  • cover medicated patch with pad
  • after 48 hours, remove medicated patch
  • repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
  • may soak corn in warm water for 5 minutes to assist in removal

Other information

OTHER SAFETY INFORMATION

store between 15°C to 30°C (59°F to 86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

​Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

​Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HILL COUNTRY ESSENTIALS
Medicated

Corn Remover
with Salicylic acid

Therapeutic Corn Removal Treatment

Protects Against Pressure & Pain

9 Pads/ Medicated Patches

Hill Country Essentials_Corn Removers_52-003HE.jpgHill Country Essentials_Corn Removers_52-003HE.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN9
240559salicylic acid 0.4 MG/MG Medicated PatchSCD9
240559salicylic acid 40 % Medicated PatchSY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-525-09Salicylic Acid9 in 1 PACKAGEPATCH99

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37808-52537808-525-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-11-17monthly-update2026-06-03 17:40:19
62024-12-10full-release2026-06-01 00:41:57

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 AcidMEDICATED CORN REMOVERSHEB553ff475-641d-4cc0-ab32-69cebec709ba2026-01-15WarningsExact identifier
ndc (package): 37808-525-09
ndc (product): 37808-525
ndc11 (package): 37808052509
spl id: 4872cf1a-dd3a-3c48-e063-6294a90aea72
spl set id: 553ff475-641d-4cc0-ab32-69cebec709ba

Reported adverse events (FAERS/openFDA)#

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