MedPath

Eucalyptol

Generic Name
Eucalyptol
Brand Names
Listerine Antiseptic
Drug Type
Small Molecule
Chemical Formula
C10H18O
CAS Number
470-82-6
Unique Ingredient Identifier
RV6J6604TK

Overview

Eucalyptol is naturally produced cyclic ether and monoterpenoid. Eucalyptol is an ingredient in many brands of mouthwash and cough suppressant. It controls airway mucus hypersecretion and asthma via anti-inflammatory cytokine inhibition. Eucalyptol is an effective treatment for nonpurulent rhinosinusitis. Eucalyptol reduces inflammation and pain when applied topically. It kills leukaemia cells in vitro.

Indication

No indication information available.

Associated Conditions

  • Gingivitis

Clinical Trials

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Big Lots
50594-664
ORAL
0.92 mg in 1 mL
5/7/2025
Target Corporation
11673-664
ORAL
0.92 mg in 1 mL
5/7/2025
TopCo Associates LLC
76162-855
ORAL
0.92 mg in 1 mL
5/7/2025
Lidl US, LLC
71141-155
ORAL
0.92 mg in 1 mL
3/24/2025
HARRIS TEETER
72036-072
ORAL
0.92 mg in 1 mL
3/3/2025
United Natural Foods, Inc. dba UNFI
41163-055
ORAL
0.92 mg in 1 mL
4/28/2025
Family Dollar (FAMILY WELLNESS)
55319-290
ORAL
0.92 mg in 1 mL
1/10/2025
Your Military Exchanges
55301-664
ORAL
0.92 mg in 1 mL
6/10/2025
Vi-Jon, LLC
0869-0664
ORAL
0.92 mg in 1 mL
5/12/2025
Topco Associates LLC
36800-664
ORAL
0.92 mg in 1 mL
5/7/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
BENTASIL GREEN
carter-horner corp.
00691585
Lozenge - Oral
0.03 %
12/31/1987
CARBOSEPTOL
herbes universelles inc.
00361593
Ointment - Topical
16 MG / G
12/31/1966
BALMINIL NASAL OINTMENT
rougier pharma division of ratiopharm inc
02135639
Ointment - Nasal
6 MG / G
12/31/1995
HOMEOPATHIC MEDICINE (S#713) DPS 30C
total health centre
02083116
Drops - Oral
30 C / ML
12/31/1994
CREO GRIPPE SUP ADULTES
produits marc-o (1987) inc., division of technilab inc.
00499501
Suppository - Rectal
.4 ML / SUP
12/30/1992
DEMO CINEOL INJ
sabex inc
00456608
Liquid - Intramuscular
184 MG / ML
12/31/1951
CAMOCARE PAIN RELIEVING CREAM
abkit inc.
01939246
Cream - Topical
3 %
12/31/1995
BALMINIL SUPPOSITORIES ADULTS
rougier pharma division of ratiopharm inc
00230553
Suppository - Rectal
200 MG
12/31/1951
CALMOMUSC LIQ
cardinaux enrg les produits naturels
00777749
Liquid - Topical
2.1 %
12/31/1989
DEMO-CINEOL ENFANTS/CHILDREN
00319724
Suppository - Rectal
185 MG
12/31/1977

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.