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 12 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sensitive Whitening Tooth-paste	POTASSIUM NITRATE, SODIUM FLUORIDE	Meijer, Inc.	c25b6a95-e604-48e3-bc55-595969d1ce9b	2025-12-23	Warnings	Exact identifier application number: M022
parodontax Active Gum Repair	STANNOUS FLUORIDE	Haleon US Holdings LLC	b51ccdd9-c0af-4caa-ad97-ad1d1423b76b	2025-12-22	Warnings	Exact identifier application number: M022
parodontax Complete Protection	STANNOUS FLUORIDE	Haleon US Holdings LLC	59bb84d6-6fd3-4586-bccf-7dc45cbbb39c	2025-12-22	Warnings	Exact identifier application number: M022
parodontax Complete Protection	STANNOUS FLUORIDE	Haleon US Holdings LLC	f6912712-ce9b-44aa-8953-b9a8d420f458	2025-12-22	Warnings	Exact identifier application number: M022
parodontax Active Gum Repair Whitening	STANNOUS FLUORIDE	Haleon US Holdings LLC	817e804c-e55e-4d77-9ab9-ff54ae794725	2025-12-22	Warnings	Exact identifier application number: M022
parodontax Active Gum Repair Breath Freshener	STANNOUS FLUORIDE	Haleon US Holdings LLC	addcb1e2-24b9-4367-adf3-6806e2439a80	2025-12-22	Warnings	Exact identifier application number: M022
parodontax	STANNOUS FLUORIDE	Haleon US Holdings LLC	0f07aa1a-97be-44af-92d8-a10777e24e0a	2025-12-22	Warnings	Exact identifier application number: M022
R B one	PHOSPHATIDYLSERINE, ZINC OXIDE	NPG Bio Pharmaceuticals Co.,Ltd.	410c40fd-cf94-0301-e063-6294a90ae2de	2025-12-18	Warnings	Exact identifier application number: M022
Dem Zero	PHOSPHATIDYLSERINE, MAGNESIUM OXIDE	NPG Bio Pharmaceuticals Co.,Ltd.	411f1a0f-ed02-cc78-e063-6394a90a0aec	2025-12-18	Warnings	Exact identifier application number: M022
Res B one	PHOSPHATIDYLSERINE, ZINC OXIDE	NPG Bio Pharmaceuticals Co.,Ltd.	21469f58-1d70-774f-e063-6294a90af039	2025-12-18	Warnings	Exact identifier application number: M022
Alzh L	PHOSPHATIDYLSERINE, MAGNESIUM OXIDE	NPG Bio Pharmaceuticals Co.,Ltd.	41056de0-aaa2-01bb-e063-6394a90af7b8	2025-12-18	Warnings	Exact identifier application number: M022
Lemon	GLYCERIN	TwinMed LLC	fc88eec0-c66c-5d6d-e053-6294a90a13d2	2025-12-18	Warnings	Exact identifier application number: M022
CloSYS	HYDROGEN PEROXIDE	Rowpar Pharmaceuticals, Inc.	299fc7b1-af6d-4bf9-810f-d35283423fe2	2025-12-17	Warnings	Exact identifier application number: M022
Ipana 20% Benzocaine Topical	BENZOCAINE	Maxill Inc.	c13761e0-d45d-4e0f-ac41-428e005f96bb	2025-12-17	Warnings	Exact identifier application number: M022
Ipana 20% Benzocaine Topical	BENZOCAINE	Maxill Inc.	6dca566b-cb6a-43c4-b6e2-f2bad77fb932	2025-12-17	Warnings	Exact identifier application number: M022
Ipana 20% Benzocaine Topical	BENZOCAINE	Maxill Inc.	f36bb9bd-e9bc-4f35-a388-e0ffadbce6ab	2025-12-17	Warnings	Exact identifier application number: M022
Ipana 20% Benzocaine Topical	BENZOCAINE	Maxill Inc.	7ede08e5-2dfe-4183-905d-28d1cea42407	2025-12-17	Warnings	Exact identifier application number: M022
Ipana 20% Benzocaine Topical	BENZOCAINE	Maxill Inc.	9de36e4f-f966-4a58-b4bf-9ac3b86b3f09	2025-12-17	Warnings	Exact identifier application number: M022
Hydrogen Peroxide	HYDROGEN PEROXIDE	CVS PHARMACY, INC	3b0ad9ac-4920-45a7-b336-dfa7f8d9bdb2	2025-12-17	Warnings	Exact identifier application number: M022
Sore Throat	PHENOL	EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)	9128d59c-6fa9-4358-865a-802257a9bd25	2025-12-16	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