American Red Cross Antiseptic

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
American Red Cross Antiseptic
Generic name
BENZALKONIUM CHLORIDE 0.13%(W/W)/BENZOCAINE 5.00%(W/W)
Manufacturer
MY IMPORTS USA LLC
Product type
HUMAN OTC DRUG
SPL set ID
421dc192-97ed-0675-e063-6394a90aa156
SPL ID
421dc19f-030c-eb14-e063-6394a90a970a
Version
1
Effective date
2025-10-27
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:37:11
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Flammable, keep away from heat, spark, electrical, fire or flame. Do not use Allergy alert: do not use this product if you have a history or allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics. When using this product When using this product: avoid contact with eyes use only as directed. Intentional misuse by deliberately concentrating and inhaling can be harmful or fatal. contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF. Stop use and ask a doctor if Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again with a few days itching, rash or irritation develops Keep out of reach of children If product is 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.