X3 Clean

Product NDC: 26550-001
11-digit product format: 265500001
Labeler code: 26550
Product ID: 26550-001_3de9253f-bb5c-71c1-e063-6294a90a71ca
Type: HUMAN OTC DRUG
Nonproprietary name: BENZALKONIUM CHLORIDE
Dosage form: AEROSOL, FOAM
Route: TOPICAL
Labeler: X3 Labs Inc.
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2009-09-01
Substance: BENZALKONIUM CHLORIDE
Active strength: 1.3 mg/mL
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 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	26550-001		D	Discontinued by firm	2026-08-11
excluded product	product	26550-001		I	Inactivated by FDA	2026-08-11
excluded package	package	26550-001	26550-001-10	D	Discontinued by firm	2026-08-11
excluded package	package	26550-001	26550-001-10	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 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		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
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	26550-001-10	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	26550-001-10	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
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	26550-001-10	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	26550-001-10	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
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	26550-001-10	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	26550-001-10	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
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	26550-001-10	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	26550-001-10	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
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	26550-001-10	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	26550-001-10	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
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	26550-001-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	26550-001-10	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
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	26550-001-10	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	26550-001-10	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
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	26550-001-10	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	26550-001-10	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
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	26550-001-10	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	26550-001-10	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
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	26550-001-10	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	26550-001-10	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
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	26550-001-10	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	26550-001-10	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
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	26550-001-10	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	26550-001-10	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	26550-001-10	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	26550-001-10	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	26550-001-10	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	26550-001-10	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	26550-001-10	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	26550-001-10	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

Additional Listing Data#

Finished product: Yes
Brand name base: X3 Clean
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	1.3 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F5UM2KM3W7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1020365	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
a8eedcfd-3b97-497a-9a34-d59b0dd78439	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
26550-001-10	2020-01-31	C162847	48780-1	9d75b9cf-d99a-f424-e053-dadaa90a57ce	X3 Hand Sanitizer (Spray)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
26550-001-12	X3 Clean	75 mL in 1 BOTTLE	AEROSOL, FOAM	75	11
26550-001-14	X3 Clean	250 mL in 1 BOTTLE	AEROSOL, FOAM	250	11
26550-001-16	X3 Clean	1000 mL in 1 BOTTLE	AEROSOL, FOAM	1000	11
26550-001-18	X3 Clean	1000 mL in 1 CARTRIDGE	AEROSOL, FOAM	1000	11
26550-001-20	X3 Clean	4000 mL in 1 BOTTLE	AEROSOL, FOAM	4000	11
26550-001-10	X3 Clean	8 mL in 1 BOTTLE	SPRAY	8	2

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Benzalkonium Chloride	ACTIVE INGREDIENT	F5UM2KM3W7	X3 CLEAN (HAND SANITIZER SPRAY) SPRAY [X3 LABS INC.]	2
Benzalkonium	ACTIVE MOIETY	7N6JUD5X6Y	X3 CLEAN (HAND SANITIZER SPRAY) SPRAY [X3 LABS INC.]	2
Cocamidopropyl Betaine	INACTIVE INGREDIENT	5OCF3O11KX	X3 CLEAN (HAND SANITIZER SPRAY) SPRAY [X3 LABS INC.]	2
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	X3 CLEAN (HAND SANITIZER SPRAY) SPRAY [X3 LABS INC.]	2
Water	INACTIVE INGREDIENT	059QF0KO0R	X3 CLEAN (HAND SANITIZER SPRAY) SPRAY [X3 LABS INC.]	2
Benzalkonium Chloride	ACTIVE INGREDIENT	F5UM2KM3W7	X3 CLEAN (HAND SANITIZER FOAM) AEROSOL, FOAM [X3 LABS INC.]	1
Benzalkonium	ACTIVE MOIETY	7N6JUD5X6Y	X3 CLEAN (HAND SANITIZER FOAM) AEROSOL, FOAM [X3 LABS INC.]	1
Cocamidopropyl Betaine	INACTIVE INGREDIENT	5OCF3O11KX	X3 CLEAN (HAND SANITIZER FOAM) AEROSOL, FOAM [X3 LABS INC.]	1
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	X3 CLEAN (HAND SANITIZER FOAM) AEROSOL, FOAM [X3 LABS INC.]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	X3 CLEAN (HAND SANITIZER FOAM) AEROSOL, FOAM [X3 LABS INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
26550-001	X3 CLEAN (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [X3 LABS INC.]	10	Current NDC, Legacy NDC, 5 package rows	20241211_a8eedcfd-3b97-497a-9a34-d59b0dd78439.zip
26550-001	X3 CLEAN (HAND SANITIZER SPRAY) SPRAY [X3 LABS INC.]	2	Current NDC, Legacy NDC, 1 package rows	20090901_cfd183f7-e2f8-44a4-a4d0-fc8823385056.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 115 · 2,294 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
antibacterial hand wipes (2257C)	ANTIBACTERIAL HAND WIPES (2257C)	Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd.	585a1c36-7bdc-4d4f-e063-6394a90ad6d2	2026-08-06	Warnings	Exact identifier application number: M003
Family Beauty Antibacterial Hand Wipes	BENZALKONIUM CHLORIDE	Zhejiang Bright Care Co., Ltd.	6ff604f7-4011-4f0e-aa2d-a46e1a973d13	2026-08-06	Warnings	Exact identifier application number: M003
antibacterial hand wipes (Angel)	ANTIBACTERIAL HAND WIPES	Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd.	585c4a14-8dc9-3a08-e063-6394a90ab4f5	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer ROSEWATER SPRITZ	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585cb4fa-6016-1550-e063-6294a90a514d	2026-08-06	Warnings	Exact identifier application number: M003
CharmTex Lightly Scented Antibacterial	BENZETHONIUM CHLORIDE	Yangzhou Jyr daily chemical Co., Ltd	4b642dfa-f044-4410-81e4-142f0497f0f3	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer PASSION MANGO SPLASH	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585df6ce-4625-d5d2-e063-6394a90a7fcb	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer LILY SPRINGS	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585e0c24-7f5f-4ba7-e063-6294a90a7597	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer WATERMELON POP	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585e3ced-fa45-8576-e063-6294a90af50f	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer ALOE BREEZE	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585e647c-2904-2d3f-e063-6394a90a2b79	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer LAVENDER DREAM	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585e8222-fad5-4409-e063-6394a90a9c60	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer JUICY APPLE	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585eb222-5495-65ed-e063-6394a90a7cfa	2026-08-06	Warnings	Exact identifier application number: M003
Hydrating Hand Sanitizer PEACH GLOW	ALCOHOL 75%	Guangzhou Ailizhuangsi Cosmetics Co., Ltd.	585ed56e-362e-7c50-e063-6394a90a1932	2026-08-06	Warnings	Exact identifier application number: M003
Isopropyl alcohol 70 percent ReadyInCase	ISOPROPYL ALCOHOL	P & L Development, LLC	57c496b3-10ab-4a72-8d8f-42a2256189dd	2026-08-06	Warnings	Exact identifier application number: M003
Wish Sanitizing Hand Wipes	BENZALKONIUM CHLORIDE	Zhejiang Bright Care Co., Ltd.	c81c0924-bb01-4fa2-b933-8777358e45e7	2026-08-05	Warnings	Exact identifier application number: M003
BBlove Hand Sanitizer JAPANESE CHERRY BLOSSOM	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	5833c261-021a-2db2-e063-6394a90a22b0	2026-08-04	Warnings	Exact identifier application number: M003
BBlove Hand Sanitizer Soft Petals	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	583438a6-c06c-87f5-e063-6394a90adec1	2026-08-04	Warnings	Exact identifier application number: M003
BBlove Hand Sanitizer Hibiscus and Aloe	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	5834801e-20e5-bffb-e063-6394a90a0359	2026-08-04	Warnings	Exact identifier application number: M003
Medi-First Antiseptic Wipes	BENZALKONIUM CHLORIDE	Unifirst First Aid Corporation	d31fe110-6d75-bf15-e053-2a95a90a8694	2026-08-03	Warnings	Exact identifier application number: M003
First Shield	HYDROGEN PEROXIDE	EVER READY FIRST AID	94307d2f-5366-4fdb-b919-4a8658dda058	2026-08-03	Warnings	Exact identifier application number: M003
BBlove Hand Sanitizer Passion Fruit Splash	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	583159a9-331a-b53b-e063-6294a90a41a3	2026-08-03	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	a8eedcfd-3b97-497a-9a34-d59b0dd78439	11
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	a8eedcfd-3b97-497a-9a34-d59b0dd78439	11
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	a8eedcfd-3b97-497a-9a34-d59b0dd78439	11
1039012	benzalkonium chloride 0.13 % Topical Spray	PSN	cfd183f7-e2f8-44a4-a4d0-fc8823385056	2
1039012	benzalkonium chloride 1.3 MG/ML Topical Spray	SCD	cfd183f7-e2f8-44a4-a4d0-fc8823385056	2
1039012	benzalkonium chloride 0.13 % Topical Spray	SY	cfd183f7-e2f8-44a4-a4d0-fc8823385056	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
26550-001-10	26550000110	8 mL in 1 BOTTLE	8 ml					Historical
26550-001-12	26550000112	75 mL in 1 BOTTLE (26550-001-12)	75 ml	2009-09-01	0000-00-00	No	No	Current
26550-001-14	26550000114	250 mL in 1 BOTTLE (26550-001-14)	250 ml	2009-09-01	0000-00-00	No	No	Current
26550-001-16	26550000116	1000 mL in 1 BOTTLE (26550-001-16)	1000 ml	2009-09-01	0000-00-00	No	No	Current
26550-001-18	26550000118	1000 mL in 1 CARTRIDGE (26550-001-18)	1000 ml	2009-09-01	0000-00-00	No	No	Current
26550-001-20	26550000120	4000 mL in 1 BOTTLE (26550-001-20)	4000 ml	2009-09-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
X3 Hand Sanitizer (Foam)	X3 Labs Inc.	2025-09-03	HUMAN OTC DRUG LABEL	11
X3 Hand Sanitizer (Spray)	X3 Labs Inc. \| Canadian Custom Packaging Company	2009-08-24	HUMAN OTC DRUG LABEL	2