Canker Care Plus

Product NDC: 70084-500
11-digit product format: 700840500
Labeler code: 70084
Product ID: 70084-500_419ce34e-1e05-d86c-e063-6294a90aade0
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol, Unspecified Form
Dosage form: LIQUID
Route: TOPICAL
Labeler: Quantum, Inc.
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2003-04-01
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 5 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	70084-500-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70084-500-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70084-500-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70084-500-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70084-500-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70084-500-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70084-500-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70084-500-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	70084-500-01	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	70084-500-01	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	70084-500-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	70084-500-01	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`

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: Canker Care Plus
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	5 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1812747	Internal RxNorm lookup
1812752	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
1ec960db-52d5-4d99-a7f7-a2e538d28724	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b82b4008-22fd-05f5-6cc6-c0a6e81c65b8	Product name	2	20240805
d206bb34-ea65-399d-70d9-834f22dc2c18	Product name	3	20170724
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-01-30	Canker Care + ®
2025-01-30	Canker Care + ®
2023-02-09	Canker Care + ®
2023-02-09	Canker Care + ®
2021-01-29	Canker Care + ®
2021-01-29	Canker Care + ®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70084-500-01	Canker Care Plus	9.7 mL in 1 BOTTLE	LIQUID	9.7		4
70084-500-01	Canker Care Plus	1 in 1 CARTON	LIQUID	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70084-500	CANKER CARE PLUS (MENTHOL, UNSPECIFIED FORM) LIQUID [QUANTUM, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20230211_1ec960db-52d5-4d99-a7f7-a2e538d28724.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 18 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Listerine Essential Care	SODIUM MONOFLUOROPHOSPHATE	Kenvue Brands LLC	90b5c3d8-baa4-44ab-8f73-e177007f0219	2025-10-10	Warnings	Exact identifier application number: M022
DuoCare Clinical Oral Rinse	CETYLPYRIDINIUM CHLORIDE	Medline Industries, LP	98e61cd5-7e29-7066-e053-2a95a90afa21	2025-10-10	Warnings	Exact identifier application number: M022
4-in-1 Teeth Care Pens	4-IN-1 TEETH CARE PENS	Jiangxi Dentalbright Technology Co., Ltd	40b756b7-ce1b-6482-e063-6294a90a0425	2025-10-09	Warnings	Exact identifier application number: M022
Giltuss Bucalsep	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Gil Pharmaceutical Corp	85053391-8d71-ab4f-e053-2991aa0a7e08	2025-10-09	Warnings	Exact identifier application number: M022
Listerine Gum Therapy Mouthwash Glacier Mint	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Kenvue Brands LLC	40a0bdf3-1698-1449-e063-6394a90ab13d	2025-10-08	Warnings	Exact identifier application number: M022
Kalaya Breath Refresh	MOUTHWASH	Avaria Health and Beauty Corp	750e99ff-72e4-3c2f-e053-2a91aa0ad5a0	2025-10-08	Warnings	Exact identifier application number: M022
Trader Joes	SODIUM FLUORIDE 0.24% AND POTASSIUM NITRATE 5%	TRADER JOE'S COMPANY	159abeba-6da2-2643-e063-6394a90a730d	2025-10-08	Warnings	Exact identifier application number: M022
Family Wellness Oral Pain Relief	BENZOCAINE 20%	FAMILY DOLLAR SERVICES INC	105d87d6-9147-43d4-e063-6394a90a57ee	2025-10-08	Warnings	Exact identifier application number: M022
Equate Glistening Mint	SODIUM FLUORIDE	Walmart Inc.	39ff21ee-a362-014e-e063-6294a90a0d91	2025-10-03	Warnings	Exact identifier application number: M022
Mouth Sore Relief Professional Strength	BENZOCAINE	CVS Pharmacy	1b7209f6-8368-47fa-8df2-b049613b8c1b	2025-09-30	Warnings	Exact identifier application number: M022
Hydrogen Peroxide	HYDROGEN PEROXIDE	Family Dollar (FAMILY WELLNESS)	9db73da2-5b70-41e6-bcf9-caa7f1142024	2025-09-29	Warnings	Exact identifier application number: M022
Esunix Oral Bacteriostatic Liquid	CETYLPYRIDINIUM CHLORIDE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f47d7e1-b6ae-efd1-e063-6394a90a4602	2025-09-27	Warnings	Exact identifier application number: M022
Chloraseptic Sore Throat Cherry	PHENOL	Prestige Brands Holdings, Inc.	d5d62f7a-8f92-4d42-a2fb-691f896f72fc	2025-09-26	Warnings	Exact identifier application number: M022
Giltuss Bucalsep	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Dextrum Laboratories Inc.	3fa233dc-156c-1e95-e063-6294a90a8bbd	2025-09-25	Warnings	Exact identifier application number: M022
Finafta MultiOral	BENZOCAINE	Dextrum Laboratories Inc.	cb027ab8-4175-4cc0-a73e-991dfb113df9	2025-09-23	Warnings	Exact identifier application number: M022
4-in-1 Teeth Care Pens	4-IN-1 TEETH CARE PENS	Jiangxi Dentalbright Technology Co., Ltd	3f872924-0c44-267b-e063-6394a90a1a67	2025-09-23	Warnings	Exact identifier application number: M022
Dental Relief	BENZOCAINE	Cintas Corporation	0f40f775-797e-43cf-88c9-00eea666494f	2025-09-23	Warnings	Exact identifier application number: M022
Seavue Anti-caries Gel	SODIUM FLUORIDE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f4c6086-b96d-8fa4-e063-6294a90ad800	2025-09-21	Warnings	Exact identifier application number: M022
Seavue Dental Desensitizer	POTASSIUM NITRATE AND SODIUM FLUORIDE DENTIFRICE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f47f399-1a14-5264-e063-6394a90aeb1c	2025-09-20	Warnings	Exact identifier application number: M022
Povi-One	POVIDONE-IODINE 10% TOPICAL	Elevate Oral Care	27c29a33-d1cc-d72f-e063-6394a90a4d45	2025-09-19	Warnings	Exact identifier application number: M022

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1812752	Canker Care 0.5 % Topical Solution	PSN	1ec960db-52d5-4d99-a7f7-a2e538d28724	4
1812747	menthol 0.5 % Topical Solution	PSN	1ec960db-52d5-4d99-a7f7-a2e538d28724	4
1812752	menthol 5 MG/ML Topical Solution [Canker Care]	SBD	1ec960db-52d5-4d99-a7f7-a2e538d28724	4
1812747	menthol 5 MG/ML Topical Solution	SCD	1ec960db-52d5-4d99-a7f7-a2e538d28724	4
1812752	Canker Care 5 MG/ML Topical Solution	SY	1ec960db-52d5-4d99-a7f7-a2e538d28724	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
70084-500-01	70084050001	1 BOTTLE in 1 CARTON (70084-500-01) / 9.7 mL in 1 BOTTLE	1 bottle	2003-04-01	No	No	Current