Alcare OR Foaming Antiseptic Handrub

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
Alcare OR Foaming Antiseptic Handrub
Generic name
ALCOHOL
Manufacturer
SC Johnson Professional USA Inc
Product type
HUMAN OTC DRUG
SPL set ID
b3a54ee6-fe64-4b48-8208-7bd586dfd089
SPL ID
47133556-34c3-456b-b3eb-e264bd064d5b
Version
2
Effective date
2025-03-14
Source export date
2026-10-27
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/a73bb3b6a943796a18cd4bcd0917240b579be4636d00e6e39481bafbd8093f69/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:36:11
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. Flammable. Keep away from fire or flame. When using this product avoid contact with eyes. If splashed in eyes, rinse promptly and thoroughly with water. do not puncture or incinerate; contents under pressure. Stop use and ask a doctor if irritation and redness develop. If irritation persists for more than 3 days, consult a physician. Keep out of reach of children In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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