Antiseptic Mouth Rinse

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
Antiseptic Mouth Rinse
Generic name
EUCALYPTOL, MENTHOL, METHYOL SALICYLATE, THYMOL
Manufacturer
Marc Glassman, Inc
Product type
HUMAN OTC DRUG
SPL set ID
47339eeb-8097-498a-ba4e-a73de477aa18
SPL ID
4a059220-3a6a-c28a-e063-6394a90a5746
Version
8
Effective date
2026-02-04
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:08:42
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings for this product Do not use if you have painful or swollen gums, pus from the gum line, loose teeth or increased spacing between the teeth. See your dentist immediately. These may be signs of periodontitis, a serious form of gum disease. Stop use and ask a dentist if gingivitis, bleeding or redness persists for more than 2 weeks. Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTION *This product is not manufactured or distributed by Johnson & Johnson Corporation, distributor of FreshBurst® Listerine® Antiseptic Mouthwash. Distributed by: Marc Glassman, Inc West 130th Street Cleveland, OH 44130 DSP-TN-21091 DSP-MO-20087

Reported adverse events (FAERS/openFDA)#

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