Antiseptic Mouth Rinse

Product NDC: 0363-0072
11-digit product format: 003630072
Labeler code: 0363
Product ID: 0363-0072_4aa43cd9-7626-e79e-e063-6294a90a6acd
Type: HUMAN OTC DRUG
Nonproprietary name: EUCALYPTOL
Dosage form: MOUTHWASH
Route: ORAL
Labeler: Walgreen Co.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2007-03-30
Substance: EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Active strength: .92; .42; .6; .64 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	0363-0072	0363-0072-12	D	Discontinued by firm	2026-10-23
excluded package	package	0363-0072	0363-0072-13	D	Discontinued by firm	2026-10-23
excluded package	package	0363-0072	0363-0072-77	D	Discontinued by firm	2026-10-23
excluded package	package	0363-0072	0363-0072-88	D	Discontinued by firm	2026-10-23

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	0363-0072-77	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	0363-0072-13	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	0363-0072-12	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	0363-0072-88	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0072-77	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0072-13	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0072-12	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0072-88	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0072-77	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0072-13	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0072-12	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0072-88	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0072-77	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0072-13	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0072-12	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0072-88	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0072-77	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0072-13	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0072-12	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0072-88	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0072-77	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0072-13	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0072-12	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0072-88	`cdf11ea48f46…`	`ba0047e9e063…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Antiseptic Mouth Rinse
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
EUCALYPTOL	.92 mg/mL
MENTHOL	.42 mg/mL
METHYL SALICYLATE	.6 mg/mL
THYMOL	.64 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
RV6J6604TK	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup
LAV5U5022Y	Internal UNII lookup
3J50XA376E	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1043619	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0363-0072-12	Antiseptic Mouth Rinse	1500 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	1500	17
0363-0072-13	Antiseptic Mouth Rinse	1250 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	1250	17
0363-0072-69	Antiseptic Mouth Rinse	250 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	250	17
0363-0072-77	Antiseptic Mouth Rinse	500 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	500	17
0363-0072-86	Antiseptic Mouth Rinse	1000 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	1000	17
0363-0072-88	Antiseptic Mouth Rinse	2000 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	2000	17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
EUCALYPTOL	ACTIVE INGREDIENT	RV6J6604TK	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
METHYL SALICYLATE	ACTIVE INGREDIENT	LAV5U5022Y	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
THYMOL	ACTIVE INGREDIENT	3J50XA376E	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
EUCALYPTOL	ACTIVE MOIETY	RV6J6604TK	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
THYMOL	ACTIVE MOIETY	3J50XA376E	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
BENZOIC ACID	INACTIVE INGREDIENT	8SKN0B0MIM	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2
SODIUM CITRATE	INACTIVE INGREDIENT	1Q73Q2JULR	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-0072	ANTISEPTIC MOUTH RINSE (EUCALYPTOL) MOUTHWASH [WALGREENS CO.]	16	Current NDC, Legacy NDC, 6 package rows	20250221_cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 72 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Family Care Anti-Itch	HYDROCORTISONE	United Exchange Corp.	8e4d46d8-7084-0666-e053-2995a90ad520	2025-10-21	Warnings	Exact identifier application number: M017
Coralite Pain Relief	CAMPHOR, MENTHOL, METHYL SALICYLATE	United Exchange Corp.	69aec845-3d4c-d226-e053-2991aa0afd12	2025-10-21	Warnings	Exact identifier application number: M017
WHITE FLOWER ANALGESIC BALM	CAMPHOR, MENTHOL AND METHYL SALICYLATE	HOE HIN PAK FAH YEOW MANUFACTORY LTD	f3e3b8b5-b12b-49ac-9318-b0c358b136e9	2025-10-21	Warnings	Exact identifier application number: M017
Mountain Ice Sports Recovery	MENTHOL	Mountainside Medical Equipment, Inc.	98638529-3c17-436e-901f-c8aea52bdab6	2025-10-20	Warnings	Exact identifier application number: M017
Lip Clear Lysine Plus	MENTHOL, UNSPECIFIED FORM	Quantum, Inc.	21a5b4fb-baed-4766-9820-5c6051c14720	2025-10-20	Warnings	Exact identifier application number: M017
Buzz Away Sting Soothe	MENTHOL	Quantum, Inc.	419e34ea-17b2-ec32-e063-6394a90a603d	2025-10-20	Warnings	Exact identifier application number: M017
Family Care Anti-Itch	HYDROCORTISONE	United Exchange Corp.	deb09e89-9794-89a7-e053-2a95a90abdf8	2025-10-20	Warnings	Exact identifier application number: M017
Numbing Cream	MENTHOL	FlexiGo Inc	41571c8f-332b-f423-e063-6394a90a8897	2025-10-20	Warnings	Exact identifier application number: M017
Soothing Nerve Therapy	MENTHOL	Wise Consumer Products	40829d6b-5005-7ec9-e063-6294a90a970e	2025-10-20	Warnings	Exact identifier application number: M017
Numbing Cream	MENTHOL	FlexiGo Inc	4146fd51-b18c-393d-e063-6294a90a4d9a	2025-10-20	Warnings	Exact identifier application number: M017
Lidocaine 4% Maximum OTC Strength	LIDOCAINE	Cardinal Health 107, LLC	975031df-d46d-4098-b1c0-1c0c92b41995	2025-10-20	Warnings	Exact identifier application number: M017
Cortizone 10 Intensive Healing	HYDROCORTISONE	Chattem, Inc.	bb3d1a3e-4c0c-4694-9c05-80152dd9bd1c	2025-10-20	Warnings	Exact identifier application number: M017
Sting relief pad	BENZOCAINE, ALCOHOL	Guangdong Comfort Medical Products Co., Ltd.	6e905065-10a9-1ded-e053-2a91aa0a46a1	2025-10-19	Warnings	Exact identifier application number: M017
CVS Cold and Hot	MENTHOL	CVS Pharmacy	a44cec95-822a-40b6-e053-2995a90ae31c	2025-10-17	Warnings	Exact identifier application number: M017
Sombra Max	SOMBRA MAX	Sombra Cosmetics Inc.	41623a46-e6e7-907e-e063-6394a90afc4c	2025-10-17	Warnings	Exact identifier application number: M017
POMADA DRAGON PAIN RELIEVING	CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE	TELEVISA CONSUMER PRODUCTS USA	c283291d-feaa-4f89-8fde-9e3957ea8b9f	2025-10-17	Warnings	Exact identifier application number: M017
Ear Pain MD	LIDOCAINE HYDROCHLORIDE	Eosera Inc	78c4418f-7f0f-447f-a94f-d4c89a081af1	2025-10-17	Warnings	Exact identifier application number: M017
WOFANLI Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	414217c1-ff3a-b556-e063-6394a90aa5db	2025-10-16	Warnings	Exact identifier application number: M017
WOFANLI Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	41422d04-160b-51b2-e063-6294a90ab2b2	2025-10-16	Warnings	Exact identifier application number: M017
WOFANLI Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	41427275-4c35-bbdf-e063-6294a90a14cf	2025-10-16	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
RV6J6604TK	EUCALYPTOL	470-82-6	EUCALYPTOL
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE
3J50XA376E	THYMOL	89-83-8	THYMOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1043619	eucalyptol 0.092 % / menthol 0.042 % / methyl salicylate 0.06 % / thymol 0.064 % Mouthwash	PSN	cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0	17
1043619	eucalyptol 0.92 MG/ML / menthol 0.42 MG/ML / methyl salicylate 0.6 MG/ML / thymol 0.64 MG/ML Mouthwash	SCD	cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0	17
1043619	eucalyptol 0.092 % / menthol 0.042 % / methyl salicylate 0.06 % / thymol 0.064 % Mouthwash	SY	cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0	17

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-0072-12	00363007212	1.5 L in 1 BOTTLE, PLASTIC (0363-0072-12)	1.5 l	2007-03-30	0000-00-00	No	No	Current
0363-0072-13	00363007213	1.25 L in 1 BOTTLE, PLASTIC (0363-0072-13)	1.25 l	2007-03-30	0000-00-00	No	No	Current
0363-0072-69	00363007269	250 mL in 1 BOTTLE, PLASTIC (0363-0072-69)	250 ml	2007-03-30	0000-00-00	No	No	Current
0363-0072-77	00363007277	.5 L in 1 BOTTLE, PLASTIC (0363-0072-77)		2007-03-30	0000-00-00	No	No	Current
0363-0072-86	00363007286	1000 mL in 1 BOTTLE, PLASTIC (0363-0072-86)	1000 ml	2007-03-30	0000-00-00	No	No	Current
0363-0072-88	00363007288	2 L in 1 BOTTLE, PLASTIC (0363-0072-88)	2 l	2007-03-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Walgreens 072.003/072AL rev 2-072AN Spring Mint Antiseptic Mouthrinse	Walgreen Co. \| Nice-Pak Products, LLC	2026-02-12	HUMAN OTC DRUG LABEL	17