Elgin Pain Relief

Product NDC: 30056-004
11-digit product format: 300560004
Labeler code: 30056
Product ID: 30056-004_2bd77bb8-2200-5994-e063-6394a90aaf77
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: GEL
Route: TOPICAL
Labeler: Eco-Logics, Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-07-11
Substance: MENTHOL
Active strength: 35 mg/g
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 40 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
2025-01-11 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	30056-004-03	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	30056-004-16	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	30056-004-32	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	30056-004-04	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	30056-004-28	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 product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
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	30056-004-28	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	30056-004-03	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	30056-004-32	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	30056-004-16	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	30056-004-04	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 product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
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	30056-004-28	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	30056-004-03	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	30056-004-32	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	30056-004-16	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	30056-004-04	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 product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
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	30056-004-28	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	30056-004-03	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	30056-004-32	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	30056-004-16	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	30056-004-04	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 product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
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	30056-004-28	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	30056-004-03	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	30056-004-32	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	30056-004-16	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	30056-004-04	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: Elgin Pain Relief
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	35 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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
808955	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
70eda21e-e566-42f4-9a49-b0d3ad000652	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDC	Effective	Indexing SPL	Related label
30056-004-03	2023-05-09	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-03	2023-05-09	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-03	2023-05-09	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-04	2023-05-09	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-04	2023-05-09	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-04	2023-05-09	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-16	2023-05-09	ba0f9c33-52e8-a910-e053-dadaa90a0b85	378d1109-6511-1f63-e054-00144ff88e88
30056-004-16	2023-05-09	ba0f9c33-52e8-a910-e053-dadaa90a0b85	378d1109-6511-1f63-e054-00144ff88e88
30056-004-16	2023-05-09	ba0f9c33-52e8-a910-e053-dadaa90a0b85	378d1109-6511-1f63-e054-00144ff88e88
30056-004-28	2023-05-09	ba0f9c33-29c8-a910-e053-dadaa90a0b85	70eda21e-e566-42f4-9a49-b0d3ad000652
30056-004-32	2023-05-09	ba0f9c33-29c8-a910-e053-dadaa90a0b85	70eda21e-e566-42f4-9a49-b0d3ad000652
30056-004-03	2021-01-29	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-03	2021-01-29	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-03	2021-01-29	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-04	2021-01-29	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-04	2021-01-29	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-04	2021-01-29	ba0f9c33-3e6d-a910-e053-dadaa90a0b85	375bfe83-c895-3ea7-e054-00144ff88e88
30056-004-16	2021-01-29	ba0f9c33-52e8-a910-e053-dadaa90a0b85	378d1109-6511-1f63-e054-00144ff88e88
30056-004-16	2021-01-29	ba0f9c33-52e8-a910-e053-dadaa90a0b85	378d1109-6511-1f63-e054-00144ff88e88
30056-004-16	2021-01-29	ba0f9c33-52e8-a910-e053-dadaa90a0b85	378d1109-6511-1f63-e054-00144ff88e88
30056-004-28	2021-01-29	ba0f9c33-29c8-a910-e053-dadaa90a0b85	70eda21e-e566-42f4-9a49-b0d3ad000652
30056-004-32	2021-01-29	ba0f9c33-29c8-a910-e053-dadaa90a0b85	70eda21e-e566-42f4-9a49-b0d3ad000652

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
30056-004-28	Elgin Pain Relief	3780 g in 1 JUG	GEL	3780	27
30056-004-32	Elgin Pain Relief	877 g in 1 BOTTLE, PUMP	GEL	877	27
30056-004-16	Elgin Pain Relief	454 g in 1 BOTTLE, PUMP	GEL	454	10
30056-004-03	Elgin Pain Relief	85 g in 1 BOTTLE, PUMP	GEL	85	7
30056-004-04	Elgin Pain Relief	113.4 g in 1 TUBE	GEL	113.4	7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Menthol	ACTIVE MOIETY	L7T10EIP3A	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Aloe Vera Leaf	INACTIVE INGREDIENT	ZY81Z83H0X	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Alpha-Tocopherol	INACTIVE INGREDIENT	H4N855PNZ1	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Camphor (Natural)	INACTIVE INGREDIENT	N20HL7Q941	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Carbomer Homopolymer Type C	INACTIVE INGREDIENT	4Q93RCW27E	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
D&C Yellow No. 10	INACTIVE INGREDIENT	35SW5USQ3G	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
FD&C Blue No. 1	INACTIVE INGREDIENT	H3R47K3TBD	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Ilex Paraguariensis Leaf	INACTIVE INGREDIENT	1Q953B4O4F	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Isopropyl Alcohol	INACTIVE INGREDIENT	ND2M416302	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Trolamine	INACTIVE INGREDIENT	9O3K93S3TK	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17
Water	INACTIVE INGREDIENT	059QF0KO0R	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
30056-004	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	27	Current NDC, Legacy NDC, 2 package rows	20250119_70eda21e-e566-42f4-9a49-b0d3ad000652.zip
30056-004	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	9	Current NDC, Legacy NDC, 1 package rows	20250119_378d1109-6511-1f63-e054-00144ff88e88.zip
30056-004	ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.]	6	Current NDC, Legacy NDC, 2 package rows	20250119_375bfe83-c895-3ea7-e054-00144ff88e88.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 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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
Medi-First Hydrocortisone 1%	HYDROCORTISONE ACETATE 1%	Unifirst First Aid Corporation	f2b46d69-1c21-5ae9-e053-2a95a90a60a9	2025-10-24	Warnings	Exact identifier application number: M017
Extra Strength	MENTHOL AND METHYL SALICYLATE	Saje Natural Business Inc.	87d872b3-3231-d0f2-e053-2995a90a9d98	2025-10-24	Warnings	Exact identifier application number: M017
Coralite Muscle and Joint Pain Relief	CAMPHOR, MENTHOL, AND MEHTYL SALICYLATE	United Exchange Corporation	78edeeb8-3e3c-64bb-e053-2a91aa0a7bbc	2025-10-24	Warnings	Exact identifier application number: M017
Coralite Odor Free Pain Relief	LIDOCAINE	United Exchange Corporation	7966d9f2-22f9-a900-e053-2991aa0aba55	2025-10-24	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
808955	menthol 3.5 % Topical Gel	PSN	70eda21e-e566-42f4-9a49-b0d3ad000652	27
808955	menthol 0.035 MG/MG Topical Gel	SCD	70eda21e-e566-42f4-9a49-b0d3ad000652	27
808955	menthol 3.5 % Topical Gel	SY	70eda21e-e566-42f4-9a49-b0d3ad000652	27
808955	menthol 3.5 % Topical Gel	PSN	378d1109-6511-1f63-e054-00144ff88e88	10
808955	menthol 0.035 MG/MG Topical Gel	SCD	378d1109-6511-1f63-e054-00144ff88e88	10
808955	menthol 3.5 % Topical Gel	SY	378d1109-6511-1f63-e054-00144ff88e88	10
808955	menthol 3.5 % Topical Gel	PSN	375bfe83-c895-3ea7-e054-00144ff88e88	7
808955	menthol 0.035 MG/MG Topical Gel	SCD	375bfe83-c895-3ea7-e054-00144ff88e88	7
808955	menthol 3.5 % Topical Gel	SY	375bfe83-c895-3ea7-e054-00144ff88e88	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
30056-004-03	30056000403	85 g in 1 BOTTLE, PUMP (30056-004-03)	85 g	2016-07-11	No	No	Current
30056-004-04	30056000404	113.4 g in 1 TUBE (30056-004-04)	113.4 g	2016-07-11	No	No	Current
30056-004-16	30056000416	454 g in 1 BOTTLE, PUMP (30056-004-16)	454 g	2016-07-11	No	No	Current
30056-004-28	30056000428	3780 g in 1 JUG (30056-004-28)	3780 g	2016-07-11	No	No	Current
30056-004-32	30056000432	877 g in 1 BOTTLE, PUMP (30056-004-32)	877 g	2016-07-11	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Menthol - Eco-Logics, Inc. \| Elginex Corporation \| Natural Essentials,Inc.	Eco-Logics, Inc. \| Elginex Corporation \| Natural Essentials,Inc.	2026-10-18	HUMAN OTC DRUG LABEL	11
Menthol - Eco-Logics, Inc. \| Elginex Corporation \| Natural Essentials,Inc.	Eco-Logics, Inc. \| Elginex Corporation \| Natural Essentials,Inc.	2026-10-18	HUMAN OTC DRUG LABEL	8
Menthol - Eco-Logics, Inc. \| Elginex Corporation \| Natural Essentials,Inc.	Eco-Logics, Inc. \| Elginex Corporation \| Natural Essentials,Inc.	2025-01-16	HUMAN OTC DRUG LABEL	27