Lidopatch

Product NDC: 10882-527
11-digit product format: 108820527
Labeler code: 10882
Product ID: 10882-527_97a56c7a-7ad6-9931-e053-2995a90a3d8e
Type: HUMAN OTC DRUG
Nonproprietary name: lidocaine, menthol
Dosage form: PATCH
Route: TOPICAL
Labeler: J.A.R. Laboratories
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2016-03-02
Marketing end: 0000-00-00
Substance: LIDOCAINE; MENTHOL
Active strength: 0 mg/1; mg/1
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 8 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	10882-527		I	Inactivated by FDA	2026-09-14
excluded product	product	10882-527		D	Discontinued by firm	2026-09-14
excluded package	package	10882-527	10882-527-03	I	Inactivated by FDA	2026-09-14
excluded package	package	10882-527	10882-527-07	I	Inactivated by FDA	2026-09-14
excluded package	package	10882-527	10882-527-30	I	Inactivated by FDA	2026-09-14
excluded package	package	10882-527	10882-527-01	D	Discontinued by firm	2026-09-14
excluded package	package	10882-527	10882-527-02	D	Discontinued by firm	2026-09-14
excluded package	package	10882-527	10882-527-04	D	Discontinued by firm	2026-09-14

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 2 · 120 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10882-527-30	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10882-527-04	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10882-527-02	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10882-527-07	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10882-527-01	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10882-527-03	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
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	10882-527-30	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	10882-527-07	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	10882-527-03	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	10882-527-30	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	10882-527-07	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	10882-527-03	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	10882-527-30	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	10882-527-07	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	10882-527-03	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	10882-527-30	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	10882-527-07	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	10882-527-03	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	10882-527-30	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	10882-527-07	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	10882-527-03	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	10882-527-30	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	10882-527-07	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	10882-527-03	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	10882-527-30	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	10882-527-07	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	10882-527-03	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	10882-527-30	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	10882-527-07	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	10882-527-03	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	10882-527-30	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	10882-527-02	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	10882-527-01	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	10882-527-07	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	10882-527-04	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	10882-527-03	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	10882-527-30	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	10882-527-02	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	10882-527-01	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	10882-527-07	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	10882-527-04	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	10882-527-03	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	10882-527-30	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	10882-527-02	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
070fbed5-7088-434a-a7ce-f2a64d8d40ac	Product name	2	20260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80f	Product name	5	20250819
860a93dc-4863-49cc-b284-6bbe8191bc48	Product name	4	20250214
eaba870a-6a9d-442e-8643-87b3f558a451	Product name	1	20250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86	Product name	1	20230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57	Product name	3	20210602
aed701d5-9c75-dfaf-7154-cde46179faea	Product name	9	20200313
fa8b5901-e681-426f-82fe-54f6d81ec698	Product name	4	20180619
332d03e4-aa24-4b11-841a-02bf41081920	Product name	1	20171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070	Product name	1	20171221
68ed98f8-24c2-44a0-944a-6d36e82ce25a	Product name	1	20141222
1cd42bc2-a430-c72b-636d-991b235fbf80	Product name	1	20140508
49fa150c-f0de-cce7-3d9c-993ed81c5698	Product name	1	20140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ff	Product name	1	20140508
9137811f-f279-8640-5aeb-99fa2145d64d	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDC	Effective	Indexing SPL	Related label
10882-527-01	2023-10-03	ba0f9c33-203c-a910-e053-dadaa90a0b85	Lidopatch
10882-527-02	2023-10-03	ba0f9c33-203c-a910-e053-dadaa90a0b85	Lidopatch
10882-527-04	2023-10-03	ba0f9c33-203c-a910-e053-dadaa90a0b85	Lidopatch
10882-527-01	2021-01-29	ba0f9c33-203c-a910-e053-dadaa90a0b85	Lidopatch
10882-527-02	2021-01-29	ba0f9c33-203c-a910-e053-dadaa90a0b85	Lidopatch
10882-527-04	2021-01-29	ba0f9c33-203c-a910-e053-dadaa90a0b85	Lidopatch
10882-527-03	2019-11-27	9855e2a2-35df-60a7-e053-dbdaa90a05bd	LidoPatch™
10882-527-07	2019-11-27	9855e2a2-35df-60a7-e053-dbdaa90a05bd	LidoPatch™
10882-527-30	2019-11-27	9855e2a2-35df-60a7-e053-dbdaa90a05bd	LidoPatch™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
10882-527-03	LidoPatchPain Relief	3 in 1 CARTON	PATCH	3	3
10882-527-03	LidoPatchPain Relief	1 in 1 POUCH	PATCH	1	3
10882-527-07	LidoPatchPain Relief	7 in 1 CARTON	PATCH	7	3
10882-527-07	LidoPatchPain Relief	1 in 1 POUCH	PATCH	1	3
10882-527-30	LidoPatchPain Relief	1 in 1 POUCH	PATCH	1	3
10882-527-30	LidoPatchPain Relief	30 in 1 CARTON	PATCH	30	3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
10882-527-03	EA - Each	10882-527	394c9e4a-034d-4dc5-a88f-699bdf867061	1	2015-05-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
lidocaine	ACTIVE INGREDIENT	98PI200987	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
menthol	ACTIVE INGREDIENT	L7T10EIP3A	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
lidocaine	ACTIVE MOIETY	98PI200987	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
menthol	ACTIVE MOIETY	L7T10EIP3A	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
COPOVIDONE K25-31	INACTIVE INGREDIENT	D9C330MD8B	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
IMIDUREA	INACTIVE INGREDIENT	M629807ATL	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
SORBITOL	INACTIVE INGREDIENT	506T60A25R	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10882-527	LIDOPATCH (LIDOCAINE, MENTHOL) PATCH [J.A.R. LABORATORIES]	13	Legacy NDC	20241204_2d139b2f-34e5-46d9-e054-00144ff8d46c.zip
10882-527	LIDOPATCH PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [JAR LABORATORIES]	3	Legacy NDC, 6 package rows	20140203_916af96b-84bf-4a1d-a000-0ccc8ea43ac5.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
98PI200987	LIDOCAINE	137-58-6	LIDOCAINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1249758	lidocaine 4 % / menthol 1 % Medicated Patch	PSN	916af96b-84bf-4a1d-a000-0ccc8ea43ac5	3
1249763	LidoPatch 4 % / 1 % Medicated Patch	PSN	916af96b-84bf-4a1d-a000-0ccc8ea43ac5	3
1249763	lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch [Lidopatch]	SBD	916af96b-84bf-4a1d-a000-0ccc8ea43ac5	3
1249758	lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch	SCD	916af96b-84bf-4a1d-a000-0ccc8ea43ac5	3
1249758	lidocaine 4 % / menthol 1 % Medicated Patch	SY	916af96b-84bf-4a1d-a000-0ccc8ea43ac5	3
1249763	LidoPatch (lidocaine 4 % / menthol 1 % ) Medicated Patch	SY	916af96b-84bf-4a1d-a000-0ccc8ea43ac5	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
10882-527-03	10882052703	3 in 1 CARTON	Historical
10882-527-07	10882052707	7 in 1 CARTON	Historical
10882-527-30	10882052730	1 in 1 POUCH	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Lidopatch	J.A.R. Laboratories	2024-12-02	HUMAN OTC DRUG LABEL	13
LidoPatch™	JAR Laboratories \| Zhuhai Guojia New Macromolecule Materiel Co., LTD	2014-01-30	HUMAN OTC DRUG LABEL	3