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
Topco Associates LLC
Product type
HUMAN OTC DRUG
SPL set ID
a38e91c1-7ac6-4a7f-a5a2-8d9166b1535a
SPL ID
4ab7ce2e-b288-955d-e063-6294a90a3a44
Version
15
Effective date
2026-02-13
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:19:04
Harmonized routes table
Harmonized routes
ORAL

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 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 DISTRIBUTED BY TOPCO ASSOCIATES LLC ITASCA, IL 60143 ©TOPCO VIJA1024 QUESTIONS? 1-888-423-0139 topcare@topco.com www.topcarebrand.com Scan here for more information or call 1-888-423-0139 QUALITY GUARANTEED DSP-TN-21091 DSP-MO-20087

Reported adverse events (FAERS/openFDA)#

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