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 102 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
K19 RELIEF	MENTHOL	K19 LLC	e2e1ca96-1ae8-4c99-b8de-ce26754292f9	2025-01-15	Warnings	Exact identifier application number: M017
Anecream	LIDOCAINE 4%	Focus Health Group	2d7706e2-7363-4047-96cb-85b718277e8c	2025-01-15	Warnings	Exact identifier application number: M017
Boroleum	CAMPHOR, MENTHOL, WHITE PETROLATUM	Reliable 1 Laboratories	846568af-0fdd-a80e-e053-2a91aa0a9c9e	2025-01-15	Warnings	Exact identifier application number: M017
LidoPro Pain Relief	CAPSAICIN AND LIDOCAINE	Advanced Rx of Tennessee, LLC	27d5997b-1cc2-41c2-e063-6394a90ac74a	2025-01-15	Warnings	Exact identifier application number: M017
Pain Relief Patch 4% Lidocaine	LIDOCAINE	Reliable 1 Laboratories LLC	2b624763-c310-63d9-e063-6394a90a1928	2025-01-15	Warnings	Exact identifier application number: M017
Cannarelief 1000mg	MENTHOL	Carolina Cannabis Creations LLC	01e2ae1a-c969-6dd2-e063-6394a90a9d9e	2025-01-15	Warnings	Exact identifier application number: M017
Healing Hand Cream 2000mg	MENTHOL	Carolina Cannabis Creations LLC	01f8795b-9f95-c793-e063-6394a90a8330	2025-01-15	Warnings	Exact identifier application number: M017
CBD Clinic Deep-Rub Pain Relief - Level 5	CAMPHOR, MENTHOL	ABACUS HEALTH PRODUCTS, INC.	31e2e5cd-d33e-f058-e063-6394a90af7d2	2025-01-14	Warnings	Exact identifier application number: M017
Meijer Odor Free Analgesic Pain Relieving Topical Analgesic	LIDOCAINE HYDROCHLORIDE	Meijer Distribution, Inc	6288efea-f636-4eea-bb9f-78aa2f9af54a	2025-01-14	Warnings	Exact identifier application number: M017
IKONIK TONIK	LIDOCAINE HYDROCHLORIDE	IKONIK CARE, LLC	122fdfe8-b5fa-46d1-9fd9-3df9887ed320	2025-01-14	Warnings	Exact identifier application number: M017
elp essential MANTECA DE UBRE	METHYL SALICYLATE, CAMPHOR	Miramar Cosmetics, Inc DBA Miramar Lab	c3964dfe-17fe-4d89-a4c4-cf500f982259	2025-01-13	Warnings	Exact identifier application number: M017
Methylten	METHYL SALICYLATE 10%	Puretek Corporation	28f4093f-803f-0e70-e063-6294a90a98a4	2025-01-13	Warnings	Exact identifier application number: M017
Refill Bundle 7 Large Office	BENZALKONIUM CHLORIDE	CMC Group, Inc.	6620a8f3-098d-d045-e053-2a91aa0a0d94	2025-01-13	Warnings	Exact identifier application number: M017
Jakwork Numbing Cream	NUMBING CREAM	Guangzhou Zanming Trading Co., Ltd.	2ba1de83-494a-6c54-e063-6294a90a9b2d	2025-01-13	Warnings	Exact identifier application number: M017
Arthritis Hot	MENTHOL AND METHYL SALICYLATE	Chattem, Inc.	cc57b9b6-8ba5-4ff3-a5df-97d8f5b1bebd	2025-01-13	Warnings	Exact identifier application number: M017
Re-Lieved Lidocaine Patch	LIDOCAINE PATCH 4%	Transfer Technology	00b40dda-53ad-0458-e063-6394a90aa835	2025-01-11	Warnings	Exact identifier application number: M017
Re-Lieved Lidocaine Patch	LIDOCAINE PATCH 4%	Transfer Technology	00b47eb7-6b43-d9e2-e063-6294a90a9a38	2025-01-11	Warnings	Exact identifier application number: M017
Re-Lieved 4% Lidocaine Fabric Tape	LIDOCAINE 4% FABRIC TAPE	Transfer Technology	e9a894b0-54f2-707e-e053-2a95a90a0f0d	2025-01-11	Warnings	Exact identifier application number: M017
Re-Lieved 3 in 1 Patch	MENTHOL, CAMPHOR, METHYL SALICYLATE PATCH	Transfer Technology	e9ab9a03-b9e3-7317-e053-2995a90a9950	2025-01-11	Warnings	Exact identifier application number: M017
ASTRAPHARM CHILLI BRAND	CAPSAICIN	Dersan Pharmaceutical Co., Ltd	b4c2d4fd-7d5d-4156-ac27-e72ebc9671ec	2025-01-10	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