Re-Lieved Lidocaine Patch

Product NDC: 71662-000
11-digit product format: 716620000
Labeler code: 71662
Product ID: 71662-000_2b73f1e8-9919-ede5-e063-6294a90ac3bd
Type: HUMAN OTC DRUG
Nonproprietary name: Lidocaine Patch 4%
Dosage form: PATCH
Route: TOPICAL
Labeler: Transfer Technology
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-07-17
Substance: LIDOCAINE
Active strength: 18 mg/116cm2
Pharmacologic classes: Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	71662-000		I	Inactivated by FDA		2026-08-11
excluded package	package	71662-000	71662-000-01	I	Inactivated by FDA		2026-08-11

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 · 22 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		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	71662-000-01	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	71662-000-01	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	71662-000-01	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	71662-000-01	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	71662-000-01	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	71662-000-01	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	71662-000-01	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	71662-000-01	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 product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
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	71662-000-06	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	71662-000-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	71662-000-20	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Additional Listing Data#

Finished product: Yes
Brand name base: Re-Lieved Lidocaine Patch
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LIDOCAINE	18 mg/116cm2

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
98PI200987	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1737778	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
00b40dda-53ad-0458-e063-6394a90aa835	Available on FDA.report

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, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71662-000-01	2025-01-30	C162847	48780-1	2cef2736-9346-d83d-e063-dadaa90ab31f	Re-Lieved Lidocaine 4% Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71662-000-01	Re-Lieved Lidocaine Patch	116 cm2 in 1 POUCH	PATCH	116	6
71662-000-01	Re-Lieved Lidocaine Patch	116 cm2 in 1 POUCH	PATCH	116	2
71662-000-01	Re-Lieved Lidocaine Patch	116 cm2 in 1 POUCH	PATCH	116	2
71662-000-06	Re-Lieved Lidocaine Patch	6 in 1 CARTON	PATCH	6	2
71662-000-20	Re-Lieved Lidocaine Patch	20 in 1 CARTON	PATCH	20	2
71662-000-01	Re-Lieved Lidocaine Patch	116 cm2 in 1 POUCH	PATCH	116	1
71662-000-01	Re-Lieved Lidocaine Patch	116 cm2 in 1 POUCH	PATCH	116	1
71662-000-01	Re-Lieved Lidocaine Patch	116 cm2 in 1 POUCH	PATCH	116	1
71662-000-05	Re-Lieved Lidocaine Patch	5 in 1 BAG	PATCH	5	1
71662-000-10	Re-Lieved Lidocaine Patch	10 in 1 PACKAGE	PATCH	10	1
71662-000-31	Re-Lieved Lidocaine Patch	31 in 1 BAG	PATCH	31	1

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71662-000-01	EA - Each	71662-000	00a56070-24c6-4880-bf29-e99cda564ab2	1	2022-09-12
71662-000-20	EA - Each	71662-000	958bdf69-3945-4f07-b11f-6fc74a4259d2	1	2023-12-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71662-000	RE-LIEVED LIDOCAINE PATCH (LIDOCAINE PATCH 4%) PATCH [TRANSFER TECHNOLOGY]	6	Current NDC, Legacy NDC, 1 package rows	20231117_b774cdf9-b413-49b5-9357-6c7573a02592.zip
71662-000	RE-LIEVED LIDOCAINE PATCH (LIDOCAINE PATCH 4%) PATCH [TRANSFER TECHNOLOGY]	2	Current NDC, Legacy NDC, 2 package rows	20250112_00b40dda-53ad-0458-e063-6394a90aa835.zip
71662-000	RE-LIEVED LIDOCAINE PATCH (LIDOCAINE PATCH 4%) PATCH [TRANSFER TECHNOLOGY]	2	Current NDC, Legacy NDC, 2 package rows	20250112_00b47eb7-6b43-d9e2-e063-6294a90a9a38.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 1 of 154 · 3,068 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	Cardinal Health, 110 dba Leader	3ed7b8a1-012f-459d-878c-813b93d4673c	2026-08-06	Warnings, Adverse reactions	Exact identifier application number: M017
Gel Cooling Pain Relief	MENTHOL	The Kroger Co.	6fb0acc8-8dab-452c-b09e-de97306e1c32	2026-08-06	Warnings, Adverse reactions	Exact identifier application number: M017
Lidocaine Tattoo Wipe	LIDOCAINE HYDROCHLORIDE	MD Tattoo Company	369c1d16-597c-e1dc-e063-6394a90a3104	2026-08-06	Warnings	Exact identifier application number: M017
Point Relief Coldspot Pain Relieving	MENTHOL	Fabrication Enterprises Inc	479fb728-4aeb-42e3-b238-f04255514baa	2026-08-05	Warnings	Exact identifier application number: M017
Lidocaine HCl	LIDOCAINE HCL	Topco Associates LLC	584e1f35-4d99-9c85-e063-6294a90ab3d0	2026-08-05	Warnings, Adverse reactions	Exact identifier application number: M017
tuiwaro LIDOCAINE Cream	LIDOCAINE CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	56e36592-a935-61d4-e063-6294a90a6e4c	2026-08-04	Warnings	Exact identifier application number: M017
Mineral Ice Extreme Menthol Pain Relief	MENTHOL	Carlin Consumer Health LLC	584f5c6e-3385-3221-e063-6294a90aabae	2026-08-04	Warnings	Exact identifier application number: M017
hydrocortisone	HYDROCORTISONE	Bryant Ranch Prepack	484fe5e4-a058-49c0-a382-c8fc3e20c3b2	2026-08-04	Warnings	Exact identifier application number: M017
procure	HYDROCORTISONE ACETATE	TWIN MED, LLC	2670c9c4-66ad-40e8-a08a-582b160de39d	2026-08-03	Warnings	Exact identifier application number: M017
Icy Hot Original Nighttime Recovery Pain Relief No Mess Roll On	MENTHOL	Chattem, Inc.	aa40c907-eeb5-4fda-b35e-439cbecc178c	2026-07-31	Warnings	Exact identifier application number: M017
Alphamale Delay Cream	BENZOCAINE	Prodigy Media Inc	53d682ee-0802-a16d-e063-6394a90aeee1	2026-07-31	Warnings	Exact identifier application number: M017
Pure Primal Delay Cream	BENZOCAINE	Prodigy Media Inc	57e9e894-c14f-d806-e063-6394a90ab8e5	2026-07-31	Warnings	Exact identifier application number: M017
Satohap	DL-CAMPHOR, L-MENTHOL, METHYL SALICYLATE	Sato Pharmaceutical Co., Ltd.	df0e2b83-8f61-4ed8-bcc4-55e4ea782090	2026-07-31	Warnings	Exact identifier application number: M017
Satogesic	DL-CAMPHOR, L-MENTHOL, METHYL SALICYLATE	Sato Pharmaceutical Co., Ltd.	cb000134-92a4-4304-8ef0-0347190e1414	2026-07-31	Warnings	Exact identifier application number: M017
Satogesic Hot	CAPSAICIN	Sato Pharmaceutical Co., Ltd.	16b47cb5-ea5f-4514-9a89-141ee4cc60f8	2026-07-31	Warnings	Exact identifier application number: M017
Satohap Cool and Hot Pads	CAMPHOR, CAPSAICIN, MENTHOL	Sato Pharmaceutical Co., Ltd.	b6bf1eab-4ab9-f500-e053-2995a90a8d7b	2026-07-31	Warnings, Adverse reactions	Exact identifier application number: M017
SATOHAP COOL and HOT	CAMPHOR, CAPSAICIN, MENTHOL	Sato Pharmaceuticals Co., Ltd.	232a4c76-1a0c-2f4b-e063-6394a90a8849	2026-07-31	Warnings, Adverse reactions	Exact identifier application number: M017
Cortizone 10 Itch Relief Massaging Rollerball	HYDROCORTISONE	Chattem, Inc.	1e27682c-f856-41f1-9935-37540960a4c7	2026-07-31	Warnings	Exact identifier application number: M017
Aspercreme with Lidocaine Dry	LIDOCAINE	Chattem, Inc.	008abaaa-5e12-4246-a7f5-66f3966acf28	2026-07-30	Warnings	Exact identifier application number: M017
ACOLYE Lidocaine Cream Topical Analgesia Cream	LIDOCAINE,MENTHOL	Guangdong Aimu Biological Technology Co., Ltd	57deebf7-52f1-4256-e063-6294a90a75d5	2026-07-30	Warnings	Exact identifier application number: M017

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
1737778	lidocaine 4 % Medicated Patch	PSN	b774cdf9-b413-49b5-9357-6c7573a02592	6
1737778	lidocaine 0.04 MG/MG Medicated Patch	SCD	b774cdf9-b413-49b5-9357-6c7573a02592	6
1737778	lidocaine 4 % Medicated Patch	SY	b774cdf9-b413-49b5-9357-6c7573a02592	6
1737778	lidocaine 4 % Medicated Patch	PSN	00b40dda-53ad-0458-e063-6394a90aa835	2
1737778	lidocaine 4 % Medicated Patch	PSN	00b47eb7-6b43-d9e2-e063-6294a90a9a38	2
1737778	lidocaine 0.04 MG/MG Medicated Patch	SCD	00b40dda-53ad-0458-e063-6394a90aa835	2
1737778	lidocaine 0.04 MG/MG Medicated Patch	SCD	00b47eb7-6b43-d9e2-e063-6294a90a9a38	2
1737778	lidocaine 4 % Medicated Patch	SY	00b47eb7-6b43-d9e2-e063-6294a90a9a38	2
1737778	lidocaine 4 % Medicated Patch	SY	00b40dda-53ad-0458-e063-6394a90aa835	2
1737778	lidocaine 4 % Medicated Patch	PSN	37ee539c-df7e-511d-e063-6394a90a4469	1
1737778	lidocaine 4 % Medicated Patch	PSN	37eef80a-556f-b090-e063-6294a90a151b	1
1737778	lidocaine 4 % Medicated Patch	PSN	37ef02d4-2ff5-cb23-e063-6294a90a68af	1
1737778	lidocaine 0.04 MG/MG Medicated Patch	SCD	37ee539c-df7e-511d-e063-6394a90a4469	1
1737778	lidocaine 0.04 MG/MG Medicated Patch	SCD	37eef80a-556f-b090-e063-6294a90a151b	1
1737778	lidocaine 0.04 MG/MG Medicated Patch	SCD	37ef02d4-2ff5-cb23-e063-6294a90a68af	1
1737778	lidocaine 4 % Medicated Patch	SY	37ee539c-df7e-511d-e063-6394a90a4469	1
1737778	lidocaine 4 % Medicated Patch	SY	37eef80a-556f-b090-e063-6294a90a151b	1
1737778	lidocaine 4 % Medicated Patch	SY	37ef02d4-2ff5-cb23-e063-6294a90a68af	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71662-000-01	71662000001	1 POUCH in 1 PACKAGE (71662-000-01) > 116 cm2 in 1 POUCH	1 pouch	2017-09-06	0000-00-00	No	No	Current
71662-000-05	71662000005	5 POUCH in 1 BAG (71662-000-05) / 116 cm2 in 1 POUCH (71662-000-01)	5 pouch	2025-06-01		No	No	Current
71662-000-06	71662000006	6 POUCH in 1 CARTON (71662-000-06) / 116 cm2 in 1 POUCH (71662-000-01)	6 pouch	2023-07-23		No	No	Current
71662-000-10	71662000010	10 POUCH in 1 PACKAGE (71662-000-10) / 116 cm2 in 1 POUCH (71662-000-01)	10 pouch	2025-06-02		No	No	Current
71662-000-20	71662000020	20 POUCH in 1 CARTON (71662-000-20) / 116 cm2 in 1 POUCH (71662-000-01)	20 pouch	2023-07-17		No	No	Current
71662-000-31	71662000031	31 POUCH in 1 BAG (71662-000-31) / 116 cm2 in 1 POUCH (71662-000-01)	31 pouch	2025-06-01		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Re-Lieved Lidocaine 4% Patch: Five pouches in a plastic bag	Transfer Technology \| Transfer Technoloy \| Akron Coating & Adhesives	2025-06-19	HUMAN OTC DRUG LABEL	1
Re-Lieved Lidocaine 4% Patch: 10 single pouches in a plastic bag	Transfer Technology \| Akron Coating & Adhesives	2025-06-19	HUMAN OTC DRUG LABEL	1
Re-Lieved Lidocaine 4% Patch: Thirty-one single pouches in a plastic bag	Transfer Technology \| Transfer Technoloy \| Akron Coating & Adhesives	2025-06-19	HUMAN OTC DRUG LABEL	1
Re-Lieved Lidocaine 4% Patch; 20 Pouches of Foam Patches per Package	Transfer Technology \| Transfer Technoloy	2025-01-11	HUMAN OTC DRUG LABEL	2
Re-Lieved Lidocaine 4% Patch, Six Foam Patches per Box	Transfer Technology \| Transfer Technoloy	2025-01-11	HUMAN OTC DRUG LABEL	2
Re-Lieved Lidocaine 4% Patch	Transfer Technology \| Transfer Technoloy \| Akron Coating & Adhesives	2023-07-28	HUMAN OTC DRUG LABEL	6