Velma Pain Relief Patch

Product NDC: 69379-016
11-digit product format: 693790016
Labeler code: 69379
Product ID: 69379-016_093efd77-4070-2006-e054-00144ff88e88
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Velma Pain Relief Patch
Dosage form: PATCH
Route: TOPICAL
Labeler: Home Aide Diagnostics, Inc.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2014-11-18
Marketing end: 0000-00-00
Substance: LIDOCAINE; MENTHOL; METHYL SALICYLATE
Active strength: 4 g/100g; g/100g; g/100g
Pharmacologic classes: Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
NDC exclude flag: E
Listing certified through: 2017-12-31
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 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	69379-016		I	Inactivated by FDA	2026-10-05
excluded package	package	69379-016	69379-016-15	D	Discontinued by firm	2026-10-05
excluded package	package	69379-016	69379-016-16	D	Discontinued by firm	2026-10-05
excluded package	package	69379-016	69379-016-17	I	Inactivated by FDA	2026-10-05

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 · 68 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	69379-016-17	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	69379-016-16	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	69379-016-16	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	69379-016-16	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	69379-016-16	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	69379-016-16	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	69379-016-16	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	69379-016-16	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	69379-016-16	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	69379-016-15	D	Discontinued by firm	`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	69379-016-17	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	69379-016-16	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	69379-016-15	D	Discontinued by firm	`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 package	package	69379-016-17	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	69379-016-16	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	69379-016-15	D	Discontinued by firm	`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 package	package	69379-016-17	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	69379-016-16	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	69379-016-15	D	Discontinued by firm	`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 package	package	69379-016-17	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	69379-016-16	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	69379-016-15	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	69379-016-17	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	69379-016-17	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	69379-016-17	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
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	69379-016-17	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	69379-016-17	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	69379-016-17	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

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
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408
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
69379-016-15	2020-01-31	C162847	48780-1	9d75b9d0-65bc-f424-e053-dadaa90a57ce	VELMA PAIN RELIEF PATCH
69379-016-16	2020-01-31	C162847	48780-1	9d75b9d0-65bc-f424-e053-dadaa90a57ce	VELMA PAIN RELIEF PATCH
69379-016-17	2020-01-31	C162847	48780-1	9d75b9d0-65bc-f424-e053-dadaa90a57ce	VELMA PAIN RELIEF PATCH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69379-016-15	Velma Pain Relief Patch	100 g in 1 PACKAGE	PATCH	100	1
69379-016-16	Velma Pain Relief Patch	15 in 1 BOX	PATCH	15	1
69379-016-16	Velma Pain Relief Patch	3 in 1 PACKAGE	PATCH	3	1
69379-016-17	Velma Pain Relief Patch	5 in 1 BOX	PATCH	5	1
69379-016-17	Velma Pain Relief Patch	3 in 1 PACKAGE	PATCH	3	1

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69379-016-17	EA - Each	69379-016	be80f2aa-90cf-4d7f-908c-9288f6e923c6	1	2015-01-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
LIDOCAINE	ACTIVE INGREDIENT	98PI200987	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
LIDOCAINE	ACTIVE INGREDIENT	98PI200987	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
LIDOCAINE	ACTIVE INGREDIENT	98PI200987	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
Methyl Salicylate	ACTIVE INGREDIENT	LAV5U5022Y	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
Methyl Salicylate	ACTIVE INGREDIENT	LAV5U5022Y	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
Methyl Salicylate	ACTIVE INGREDIENT	LAV5U5022Y	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
LIDOCAINE	ACTIVE MOIETY	98PI200987	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
LIDOCAINE	ACTIVE MOIETY	98PI200987	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
LIDOCAINE	ACTIVE MOIETY	98PI200987	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69379-016	VELMA PAIN RELIEF PATCH PATCH [HOME AIDE DIAGNOSTICS, INC.]	1	Legacy NDC, 5 package rows	20141202_093efd77-406f-2006-e054-00144ff88e88.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
98PI200987	LIDOCAINE	137-58-6	LIDOCAINE
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1599163	lidocaine 4 % / menthol 2 % / methyl salicylate 16 % Medicated Patch	PSN	093efd77-406f-2006-e054-00144ff88e88	1
1599163	lidocaine 0.04 MG/MG / menthol 0.02 MG/MG / methyl salicylate 0.16 MG/MG Medicated Patch	SCD	093efd77-406f-2006-e054-00144ff88e88	1
1599163	lidocaine 4 % / menthol 2 % / methyl salicylate 16 % Medicated Patch	SY	093efd77-406f-2006-e054-00144ff88e88	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Status
69379-016-15	69379001615	100 g in 1 PACKAGE	100 g	Historical
69379-016-16	69379001616	15 in 1 BOX		Historical
69379-016-17	69379001617	5 in 1 BOX		Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
VELMA PAIN RELIEF PATCH	Home Aide Diagnostics, Inc.	2014-12-02	HUMAN PRESCRIPTION DRUG LABEL	1
VELMA PAIN RELIEF PATCH	Home Aide Diagnostics, Inc.	2014-11-26	HUMAN PRESCRIPTION DRUG LABEL	1
VELMA PAIN RELIEF PATCH	Home Aide Diagnostics, Inc.	2014-11-18	HUMAN PRESCRIPTION DRUG LABEL	1