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 22 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hydrogen Peroxide 3 Percent	HYDROGEN PEROXIDE	WinCo Foods, LLC	9417b340-942b-48bf-bbfd-4cd5154082b9	2025-02-12	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	b291811f-8fac-45e2-a9a2-b3ecc0813d0d	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	fea30599-5e3b-4163-9660-d41b3fcee143	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	3be68966-199c-481e-8b9e-e994c41fd96a	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	ccdee0cc-2bc9-4165-a411-02f4f900d86a	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	0ca2b042-ea2c-4cbe-ae68-5a72a6bfa0b7	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	69c4dd1b-a0db-4495-bfc3-faffdfdf59bf	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	d5ef3e65-35e8-4323-9f33-3076b561e105	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	746df21c-e92e-4a71-b1c6-baf99785a43e	2025-01-29	Warnings	Exact identifier application number: M022
NRG Topical Anesthetic	BENZOCAINE	IQ Dental Supply, LLC	2345e614-c7b6-448c-8e07-31700bade91c	2025-01-29	Warnings	Exact identifier application number: M022
UltraCare Anesthetic Gel	BENZOCAINE	The Belport Company, Inc. DBA Gingi-Pak	142062ca-6f8f-78d2-e063-6294a90a19d8	2025-01-29	Warnings, Adverse reactions	Exact identifier application number: M022
CHLORASEPTIC MAX	MENTHOL AND BENZOCAINE	Prestige Brands Holdings, Inc.	edd12a2d-aa27-4f15-9ce6-862e4b6144c4	2025-01-23	Warnings	Exact identifier application number: M022
meijer Sensitive FRESH MINT	POTASSIUM NITRATE, SODIUM FLUORIDE	Meijer, Inc.	bea36d55-1a5d-40c0-b422-92fb36043ee6	2025-01-23	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic	BENZOCAINE	Beutlich Pharmaceuticals, LLC	159d412c-6d1a-45d4-88c0-8c93960f946e	2025-01-21	Warnings	Exact identifier application number: M022
SEACALL Mouthwash	MOUTHWASH	Guangdong Quadrant Ecological Technology Co., Ltd.	2c1a7eed-6a7c-eeb2-e063-6394a90aafcc	2025-01-19	Warnings	Exact identifier application number: M022
BENZOCAINE Raspberry	BENZOCAINE	Darby Dental Supply, LLC	dd805400-26c5-4c18-ade2-821298233f9b	2025-01-17	Warnings	Exact identifier application number: M022
KAYLAAN	ZERO WASTE REFILL FOR TOOTHPASTE	Kaylaan LLC	c68fd8c7-7ec3-cc3f-e053-2995a90a4395	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	d22f7776-1b3c-4744-bcfe-8d9597218d73	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	9c6a26e8-1253-49f7-9ce2-45c0d39f05c5	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	48178733-7433-41ec-b178-1314e0edab1a	2025-01-16	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