Dr Lift Antibacterial Hand Sanitizer

Product NDC: 68062-2250
11-digit product format: 680622250
Labeler code: 68062
Product ID: 68062-2250_436f3a5d-a6a3-615c-e063-6394a90abd10
Type: HUMAN OTC DRUG
Nonproprietary name: ethyl alcohol
Dosage form: GEL
Route: TOPICAL
Labeler: Spa de Soleil
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-07-29
Substance: ALCOHOL
Active strength: 168 mL/240mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 22 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	68062-2250-1	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	68062-2250-1	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	68062-2250-1	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	68062-2250-1	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	68062-2250-1	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	68062-2250-1	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	68062-2250-1	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	68062-2250-1	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	68062-2250-1	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	68062-2250-1	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	68062-2250-1	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: Dr Lift Antibacterial Hand Sanitizer
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	168 mL/240mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
581662	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
aba006cd-18db-e42f-e053-2995a90a4607	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68062-2250-1	Dr Lift Antibacterial Hand Sanitizer	240 mL in 1 BOTTLE, PUMP	GEL	240		3

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 97 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Alcohol sterile	ISOPROPYL ALCOHOL	Cardinal Health, Inc	bb7c530f-5d80-4158-b715-09c1c837299d	2024-11-21	Warnings	Exact identifier application number: M003
Alcohol sterile	ISOPROPYL ALCOHOL	Cardinal Health 200 LLC	10135db9-f614-4511-96ac-faa6a02a1b61	2024-11-21	Warnings	Exact identifier application number: M003
BZK Antiseptic Swabsticks 4 Triple	BENZALKONIUM CHLORIDE	Changzhou Maokang Medical Products Co., Ltd	d9f35c14-2f5a-4e1a-bc2b-a7e163134213	2024-11-21	Warnings	Exact identifier application number: M003
Povidone-lodine Swabsticks Triple	POVIDONE-IODINE	Changzhou Maokang Medical Products Co., Ltd	74e70ea9-640b-4295-a40f-56f65fca1300	2024-11-21	Warnings	Exact identifier application number: M003
MK Alcohol Prep Pads Medium	ISOPROPYL ALCOHOL	Changzhou Maokang Medical Products Co., Ltd	37f10b1f-b73c-4d71-91c2-1252f3d9d4ce	2024-11-21	Warnings	Exact identifier application number: M003
BZK Antiseptic Towelette	BENZALKONIUM CHLORIDE	Changzhou Maokang Medical Products Co., Ltd	1936d749-bf38-a433-e063-6294a90aba8c	2024-11-21	Warnings	Exact identifier application number: M003
Maokang 10 Povidone Iodine	POVIDONE-IODINE	Changzhou Maokang Medical Products Co., Ltd	7c17ce40-0358-44ff-aa60-53711666914b	2024-11-21	Warnings	Exact identifier application number: M003
MK Alcohol Prep Pads Medium	ISOPROPYL ALCOHOL	Changzhou Maokang Medical Products Co., Ltd	11390854-9e72-40a2-9c89-3c29a585dced	2024-11-21	Warnings	Exact identifier application number: M003
Instant Hand Sanitizeing Wipe	ISOPROPANOL AND COMPOUND DOUBLE-STRANDED QUATERNARY AMMONIUM SALTS	Shandong Yayun Sanitary Products Co., Ltd.	aa0dc01a-2c6b-7402-e053-2a95a90af6a2	2024-11-21	Warnings	Exact identifier application number: M003
Dynarex Povidone Iodine Prep Solution	POVIDONE IODINE PREP SOLUTION	Dynarex Corporation	6bb4d55b-2be7-3549-e053-2a91aa0a2bb0	2024-11-20	Warnings	Exact identifier application number: M003
Dynarex Povidone Iodine Surgical Scrub	POVIDONE IODINE SURGICAL SCRUB SOLUTION	Dynarex Corporation	6f053e55-cbf6-9072-e053-2991aa0a2edd	2024-11-20	Warnings	Exact identifier application number: M003
Dynarex Green	ALCOHOL	Dynarex Corporation	072572be-49dd-4594-bc40-b56db57ada5b	2024-11-20	Warnings	Exact identifier application number: M003
Dynarex Green	CHLOROXYLENOL	Dynarex Corporation	59b098d2-08de-4fdb-a209-ae226abf37d6	2024-11-20	Warnings	Exact identifier application number: M003
Baby Wipes	PROPYLENE GLYCOL	Shandong Yayun Sanitary Products Co., Ltd.	aeb9a12c-955f-5030-e053-2995a90a2dd6	2024-11-20	Warnings	Exact identifier application number: M003
Pet wipes	BENZALKONIUM CHLORIDE	Shandong Yayun Sanitary Products Co., Ltd.	2764ea79-32d8-b7f6-e063-6394a90a5501	2024-11-20	Warnings	Exact identifier application number: M003
Premium Hand Sanitizer	ETHANOL	MCKESSON MEDICAL-SURGICAL INC.	a9514466-e0c6-4792-984a-9f07d94ee887	2024-11-18	Warnings	Exact identifier application number: M003
MARVEL BZK ANTISEPTIC WIPE	BENZALKONIUM CHLORIDE	Ashtel Studios, Inc.	93ed0bb4-834d-44ca-9c0a-20086fc09ab8	2024-11-18	Warnings	Exact identifier application number: M003
Isopropyl Rubbing Alcohol	ISOPROPYL ALCOHOL	McKesson Medical-Surgical Inc.	98b0bcc2-539b-4471-ba98-bbe17bb881bd	2024-11-15	Warnings	Exact identifier application number: M003
CVS Health Hydrogen Peroxide Wipes	HYDROGEN PEROXIDE	CVS PHARMACY, INC	7a930a5e-5b69-428f-9cbb-d03dae180295	2024-11-12	Warnings	Exact identifier application number: M003
First Aid Only Povidone-Iodine Prep Pad	POVIDONE-IODINE	Acme United Corporation	509b6c8e-6a9f-2656-e054-00144ff8d46c	2024-11-09	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
581662	ethanol 70 % Topical Gel	PSN	aba006cd-18db-e42f-e053-2995a90a4607	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	aba006cd-18db-e42f-e053-2995a90a4607	3
581662	ethanol 70 % Topical Gel	SY	aba006cd-18db-e42f-e053-2995a90a4607	3
581662	ethyl alcohol 70 % Topical Gel	SY	aba006cd-18db-e42f-e053-2995a90a4607	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68062-2250-1	68062225001	240 mL in 1 BOTTLE, PUMP (68062-2250-1)	240 ml	2020-07-29	0000-00-00	No	No	Current