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 63 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
After Bite Outdoor	DIPHENHYDRAMINE HCL	Tender Corporation d/b/a Adventure Ready Brands	22b891a9-6386-dee1-e063-6394a90a5c2f	2025-11-14	Warnings	Exact identifier application number: M017
QR PAIN	ANALGESIC	MARYHELENE ENTERPRISES INC	8f8f53e3-fe31-e7b5-e053-2995a90a710d	2025-11-14	Warnings	Exact identifier application number: M017
QR PAIN	ANALGESIC	MARYHELENE ENTERPRISES INC	9984a510-30be-4013-e053-2995a90a841e	2025-11-14	Warnings	Exact identifier application number: M017
Anti-Itch Cream	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	Kroger	3f881349-fcdd-e276-e063-6394a90ae49e	2025-11-13	Warnings	Exact identifier application number: M017
Rapid Relief	PLANTAR FASCIITIS PAIN RELIEF LIDOCAINE 4% MENTHOL 1%	RAPID AID VIET NAM COMPANY LIMITED	434cb8b2-a996-5360-e063-6394a90ada03	2025-11-13	Warnings	Exact identifier application number: M017
Rapid Relief	COLD RELIEF PATCH 5% MENTHOL	RAPID AID VIET NAM COMPANY LIMITED	4360e3ec-7a4b-b28e-e063-6294a90a0bd6	2025-11-13	Warnings	Exact identifier application number: M017
Rapid Relief	PAIN RELIEF PATCH CAMPHOR 110MG MENTHOL 33MG CAPSICUM EXTRACT 22MG	RAPID AID VIET NAM COMPANY LIMITED	4360e3be-0ec4-cd57-e063-6394a90aca63	2025-11-13	Warnings	Exact identifier application number: M017
Rapid Relief	PAIN RELIEF PATCH LIDOCAINE 4% MENTHOL 1%	RAPID AID VIET NAM COMPANY LIMITED	43616ad7-58bb-e5ad-e063-6394a90a192b	2025-11-13	Warnings	Exact identifier application number: M017
4x Medicated Severe Toothache and Gum Gel	BENZALKONIUM CHLORIDE	Meijer	97ce7890-5093-1763-e053-2a95a90afae7	2025-11-13	Warnings	Exact identifier application number: M017
Pain Reliever	CAMPHOR, MENTHOL	Kool 'N Fit Inc.	2253f6bd-5707-b993-e063-6394a90aa74a	2025-11-13	Warnings	Exact identifier application number: M017
Rapid Relief	PLANTAR FASCIITIS PAIN RELIEF LIDOCAINE 4% MENTHOL 1%	RAPID AID VIET NAM COMPANY LIMITED	4360e0d1-46cd-ab4b-e063-6394a90a55e1	2025-11-12	Warnings	Exact identifier application number: M017
CVS Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	CVS	8723e097-296f-784a-e053-2991aa0a552e	2025-11-12	Warnings	Exact identifier application number: M017
Dragon Pain Relieving Balm	CAMPHOR, MENTHOL	Americanna Wellness, Inc.	154d8821-3e76-b0e2-e063-6294a90ae077	2025-11-12	Warnings	Exact identifier application number: M017
Good neighbor Pharmacy Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	AMERISOURCEBERGEN DRUG CORPORATION	87395273-380c-7cef-e053-2991aa0a54c6	2025-11-12	Warnings	Exact identifier application number: M017
Quality Choice Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	Chain Drug Marketing Association	8735b298-83f3-0b5d-e053-2a91aa0a8292	2025-11-12	Warnings	Exact identifier application number: M017
Dragon Pain Relieving Balm	CAMPHOR, MENTHOL	Americanna Wellness, Inc.	1550e794-b3c0-4769-e063-6294a90a8c2d	2025-11-12	Warnings	Exact identifier application number: M017
Dragon Pain Relieving Balm	CAMPHOR, MENTHOL	Americanna Wellness, Inc.	154fd46e-f00d-1772-e063-6394a90aba7d	2025-11-12	Warnings	Exact identifier application number: M017
Best Choice Itch Stopping	DIPHENHYDRAMINE HCL	Valu Merchandisers	884cfd64-2cd1-8c12-e053-2995a90a8925	2025-11-12	Warnings	Exact identifier application number: M017
Itch Stopping	DIPHENHYDRAMINE HCL	CVS	8839149d-e6d5-57cc-e053-2995a90a9832	2025-11-12	Warnings	Exact identifier application number: M017
Itch Stopping	DIPHENHYDRAMINE HCL	Chain Drug Marketing Association	884c9b47-d511-1d17-e053-2995a90a42eb	2025-11-12	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