Lip Clear Lysine Plus

Product NDC: 70084-320
11-digit product format: 700840320
Labeler code: 70084
Product ID: 70084-320_419d00d6-7f99-7348-e063-6394a90a38cd
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol, Unspecified Form
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Quantum, Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1984-10-01
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 1 mg/g
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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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	70084-320-07	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: Lip Clear Lysine Plus
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	1 mg/g

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
1812680	Internal RxNorm lookup
1812685	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
21a5b4fb-baed-4766-9820-5c6051c14720	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
60c52429-fcef-eb54-2387-43bc9e4f296b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-01-30	Lip Clear ® Lysine + ®
2025-01-30	Lip Clear ® Lysine + ®
2023-02-09	Lip Clear ® Lysine + ®
2023-02-09	Lip Clear ® Lysine + ®
2021-01-29	Lip Clear ® Lysine + ®
2021-01-29	Lip Clear ® Lysine + ®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70084-320-07	Lip Clear Lysine Plus	1 in 1 CARTON	OINTMENT	1		4
70084-320-07	Lip Clear Lysine Plus	7 g in 1 TUBE	OINTMENT	7		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70084-320	LIP CLEAR LYSINE PLUS (MENTHOL, UNSPECIFIED FORM) OINTMENT [QUANTUM, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20230211_21a5b4fb-baed-4766-9820-5c6051c14720.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 70 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
RELISPRAY NATURAL PAIN RELIEF	MENTHOL	Midas-Care Pharmaceuticals, Pvt. Ltd	adc8a43c-19a1-4eb3-9820-b63f7b5e91ea	2025-10-30	Warnings	Exact identifier application number: M017
Aveeno Anti-Itch Concentrated	ZINC OXIDE, FERRIC OXIDE RED, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	07f4d4d0-9cee-46c3-bc71-2024abd31c9e	2025-10-29	Warnings	Exact identifier application number: M017
zourunan Relieve itching cream ANTIFUNGAL	RELIEVE ITCHING CREAM	Guchutang Biotechnology (Longyan) Co., Ltd	41bb9ced-dde4-2998-e063-6394a90a8159	2025-10-29	Warnings	Exact identifier application number: M017
zourunan Intensive healing lotion. for ECZEMA	INTENSIVE HEALING LOTION	Guchutang Biotechnology (Longyan) Co., Ltd	41bad9f3-f1a7-e92c-e063-6394a90ad0ba	2025-10-29	Warnings	Exact identifier application number: M017
Aromalief Pain Relief Cream Orange Ginger	MENTHOL	Marketites LLC	9e8d3611-ef1b-4ac6-e053-2995a90af28a	2025-10-29	Warnings	Exact identifier application number: M017
Aromalief Calming Pain Relief Cream Lavender	MENTHOL	Marketites LLC	b8197d52-ccfb-b008-e053-2995a90a0a53	2025-10-29	Warnings	Exact identifier application number: M017
Aromalief Cozy Vanilla Pain Relief Cream	MENTHOL	Marketites LLC	3634e55e-8c62-a782-e063-6394a90a6508	2025-10-29	Warnings	Exact identifier application number: M017
BENOVA PAIN AND ITCH RELIEF	MENTHOL, 0.11%	BENOVA RX LLC	42513ee2-8b40-a9f3-e063-6394a90a9386	2025-10-29	Warnings	Exact identifier application number: M017
Burn Relief	LIDOCAINE	CVS Pharmacy	7e9285fd-26d5-3eac-e053-2991aa0ae2db	2025-10-29	Warnings	Exact identifier application number: M017
Coralite Ultra Strength Pain Relief	CAMPHOR MENTHOL	United Exchange Corp.	44ecf959-cc07-4adc-a500-075b2ee69548	2025-10-29	Warnings	Exact identifier application number: M017
GoodSense Pain Relief	LIDOCAINE	Geiss, Destin & Dunn, Inc	826f8da4-8468-ea0a-e053-2991aa0a66cb	2025-10-28	Warnings	Exact identifier application number: M017
CALMADOL	CAMPHOR, MENTHOL, METHYL SALICYLATE	GRANDALL DISTRIBUTING, LLC	31b7f84e-8b66-4d31-8e9c-279d0af2fe64	2025-10-28	Warnings	Exact identifier application number: M017
XRay DOL	CAMPHOR, MENTHOL, AND METHYL SALICYLATE	Genomma Lab USA, Inc.	e07fef46-68d9-769c-e053-2a95a90aa065	2025-10-28	Warnings	Exact identifier application number: M017
CVS Medicated Heat	CAPSICUM EXTRACT	CVS Pharmacy	81cd1019-93a6-311b-e053-2991aa0a7997	2025-10-28	Warnings	Exact identifier application number: M017
Foster and Thrive	LIDOCAINE	STRATEGIC SOURCING SERVICES, LLC	f950b072-d978-b629-e053-6394a90abfaf	2025-10-28	Warnings	Exact identifier application number: M017
Calamine Plus Pramoxine HCl	CALAMINE PLUS SPRAY	Premier Brands of America, Inc.	d3452573-f91f-f157-e053-2a95a90a1ad8	2025-10-27	Warnings	Exact identifier application number: M017
PR	MENTHOL	Amphp, Inc	6f5b9e08-c445-4fac-e053-2a91aa0aa737	2025-10-27	Warnings	Exact identifier application number: M017
Lidocaine	BURN RELIEF	Foodhold USA	b25dc0df-02d0-41ac-b36c-2c04baa77ef2	2025-10-27	Warnings	Exact identifier application number: M017
Menthol	MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE	FSA Store Inc.	fb3548c8-f202-dc50-e053-6394a90a5b30	2025-10-27	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE CONTINUOUS SPRAY	Premier Brands of America, Inc.	d344f68b-9b62-3029-e053-2995a90a1665	2025-10-27	Warnings	Exact identifier application number: M017

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
1812685	Lysine Plus 0.1 % Topical Ointment	PSN	21a5b4fb-baed-4766-9820-5c6051c14720	4
1812680	menthol 0.1 % Topical Ointment	PSN	21a5b4fb-baed-4766-9820-5c6051c14720	4
1812685	menthol 0.001 MG/MG Topical Ointment [Lysine Plus]	SBD	21a5b4fb-baed-4766-9820-5c6051c14720	4
1812680	menthol 0.001 MG/MG Topical Ointment	SCD	21a5b4fb-baed-4766-9820-5c6051c14720	4
1812685	Lysine Plus 0.1 % Topical Ointment	SY	21a5b4fb-baed-4766-9820-5c6051c14720	4
1812680	menthol 0.1 % Topical Ointment	SY	21a5b4fb-baed-4766-9820-5c6051c14720	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
70084-320-07	70084032007	1 TUBE in 1 CARTON (70084-320-07) / 7 g in 1 TUBE	1 tube	1984-10-01	No	No	Current