Alcare OR Foamed 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 Foamed Antiseptic Handrub
Generic name
ALCOHOL
Manufacturer
SC Johnson Professional USA, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
acc2f83f-6b9b-4552-8330-33e7b99397d8
SPL ID
2bb9aa00-e7ed-46d0-9092-4e1f4a26d0bc
Version
3
Effective date
2024-12-20
Source export date
2026-08-01
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 22:59:38
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.