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 30 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Patterson Dental Topical Anesthetic	BENZOCAINE	Patterson Dental	72fd2232-cd5a-4e25-b139-522b589c4472	2025-01-08	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic	BENZOCAINE	Beutlich Pharmaceuticals, LLC	42521b29-67e4-4a16-848d-7e6ba4a7ece2	2025-01-08	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic	BENZOCAINE	Beutlich Pharmaceuticals LLC	723da3ae-3f1f-4962-920b-f2a30c8c3253	2025-01-08	Warnings, Adverse reactions	Exact identifier application number: M022
V34 Colour Corrector	V34 COLOUR CORRECTOR	Jiangxi Dentalbright Technology Co., Ltd	2b2a0b47-7628-4b85-e063-6294a90a45a0	2025-01-07	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	bc2e7ac3-f9e4-49cc-9f0c-6fe94479314d	2025-01-03	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	fb38b10d-0faf-403c-9921-d4f6b0f6aa55	2025-01-03	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	a9dc2245-c029-4453-bfc5-8fb899873c34	2025-01-03	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	ba49a18d-8568-421b-a495-8fee863c9757	2025-01-03	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	c9b584d9-7407-445a-b084-926250af9f8e	2025-01-03	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	4aa6eec8-394a-4ecb-8173-66561fd64913	2025-01-03	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	25c99ae3-90f4-4a63-924d-f810b3ba6e60	2025-01-03	Warnings	Exact identifier application number: M022
Benzo-Jel	BENZOCAINE	Henry Schein Inc.	84e8d5c8-2a35-4179-9a9c-9a4a52c2cae6	2025-01-03	Warnings	Exact identifier application number: M022
Prevention Oncology Mouth Rinse	GLYCERIN	Prevention Health Sciences, Inc.	1ec9ed1c-bcb6-3a0a-e054-00144ff8d46c	2025-01-01	Warnings	Exact identifier application number: M022
Prevention Mouth Sore Rinse	HYDROGEN PEROXIDE	Prevention Health Sciences, Inc.	2eae61e4-1800-5fa6-e063-6394a90a9583	2025-01-01	Warnings	Exact identifier application number: M022
Antiseptic Lil Drug Store Products	EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOL	Lil' Drug Store Products, Inc	dca36a30-2c9f-4d0b-be88-b45c7046f509	2024-12-31	Warnings	Exact identifier application number: M022
Sensodyne Clinical White Intensive Clean	POTASSIUM NITRATE, SODIUM FLUORIDE	Haleon US Holdings LLC	f193ec40-032f-42c7-81f1-029ec8989374	2024-12-31	Warnings	Exact identifier application number: M022
TeethWhitening Kit	TEETHWHITENING KIT	Jiangxi Dentalbright Technology Co., Ltd.	29393313-217a-dc3a-e063-6294a90addb1	2024-12-20	Warnings	Exact identifier application number: M022
Breezers Cool Berry	PECTIN	Mondelez Global LLC	b31d0078-21d7-4d18-a8d3-7c8d48d6d004	2024-12-20	Warnings	Exact identifier application number: M022
Breezers Creamy Strawberry	PECTIN	Mondelez Global LLC	777fd6db-f129-4489-8312-4b1aca94878e	2024-12-20	Warnings	Exact identifier application number: M022
Halls Breezers Sugar Free Cool Berry	PECTIN	Mondelez Global LLC	dd1b4b17-4f73-4052-9589-d5fd6bb059bb	2024-12-20	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