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 23 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	af430cf4-f1b4-4b57-b8e3-87df96d655d3	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	2b089fec-cae3-4dc9-964d-d37f732a2f9f	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	6c137a93-4a34-4849-997f-bd0c572466ef	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	e8aa9709-e8f6-47a6-ab29-1fef2309786b	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	8c55b39c-8231-46a1-92ef-9fb4e3f40c1e	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	9e82dc54-aeca-457f-b4b9-2f18cc269538	2025-01-16	Warnings	Exact identifier application number: M022
Pearson Topical Anesthetic	BENZOCAINE	Pearson Dental Supplies INC.	1a8f5964-770a-4d14-a7b6-18b5da9159b0	2025-01-16	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.	d722cdf3-7671-eb27-e053-2a95a90a09c4	2025-01-16	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.	d722bf24-ae85-54f6-e053-2995a90a1d35	2025-01-16	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.	d721864d-0950-8379-e053-2a95a90a3bcb	2025-01-16	Warnings	Exact identifier application number: M022
Defend	BENZOCAINE	Mydent International	b0e5dc67-da7a-42ac-8657-e8e4da6914be	2025-01-16	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.	d721ff57-0111-4bbb-e053-2995a90a1a70	2025-01-16	Warnings	Exact identifier application number: M022
Defend	BENZOCAINE	Mydent International	8129e871-5f31-4138-ae47-f8978fa6287f	2025-01-16	Warnings	Exact identifier application number: M022
Defend	BENZOCAINE	Mydent International	0301c1bc-db48-4635-97f5-9eaef7ab9579	2025-01-16	Warnings	Exact identifier application number: M022
Defend	BENZOCAINE	Mydent International	c0c88180-ccdc-4c48-b262-3ec20d4775d4	2025-01-16	Warnings	Exact identifier application number: M022
Defend	BENZOCAINE	Mydent International	ba011795-6822-4fff-b9c8-5c91cf9972a7	2025-01-16	Warnings	Exact identifier application number: M022
Defend	BENZOCAINE	Mydent International	1c6d5e87-3fad-4a2c-9e5f-96166d0beaeb	2025-01-16	Warnings	Exact identifier application number: M022
Defend	BENZOCAINE	Mydent International	462a5f09-131f-4dfa-a502-547c44e4a4a5	2025-01-16	Warnings	Exact identifier application number: M022
Benzocaine	TOPICAL ANESTHETIC	Everpharm LLC	2bc57111-0f15-b237-e063-6294a90a4471	2025-01-15	Warnings	Exact identifier application number: M022
Kanka Triple Action	BENZOCAINE AND MENTHOL, UNSPECIFIED FORM	Blistex Inc.	078fcdab-38a1-4a9a-bdd3-e17446591ea8	2025-01-09	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