Medicated Callus Removers

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Medicated Callus Removers
Generic name
SALICYLIC ACID
Manufacturer
Premier Brands of America Inc
Product type
HUMAN OTC DRUG
SPL set ID
52d0b36c-b65e-00cf-e063-6294a90ad089
SPL ID
52d0b459-aa10-27a6-e063-6294a90ac58f
Version
1
Effective date
2026-05-27
Source export date
2026-10-30
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/57469fe40e5b1c0d9604dc7dbc22532ea48e8e53acfb911fc676578d98492f7e/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:29:44
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use if you are a diabetic if you have poor blood circulation on irritated skin or on any area that is infected or reddened 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 right away.

Reported adverse events (FAERS/openFDA)#

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