FOOTSPA PEDI

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
FOOTSPA PEDI
Generic name
ALCOHOL
Manufacturer
CHEMCO CORPORATION
Product type
HUMAN OTC DRUG
SPL set ID
3886a958-d035-ed15-e063-6294a90af1b5
SPL ID
4c25a816-65f9-6189-e063-6294a90a4d04
Version
2
Effective date
2026-03-03
Source export date
2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:46
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

For external use only. Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Stop use and ask a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor. For external use only. Do not use on wounds or damaged skin, with a heating pad or on a child under 12 years of age

Reported adverse events (FAERS/openFDA)#

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