Dr Lift Advanced Antibacterial Wipes

Product NDC: 68062-2244
11-digit product format: 680622244
Labeler code: 68062
Product ID: 68062-2244_50b715dd-873e-7d39-e063-6294a90a861d
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: LIQUID
Route: TOPICAL
Labeler: Spa de Soleil
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-09-17
Substance: BENZALKONIUM CHLORIDE
Active strength: .156 mg/120mg
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 · 18 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		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	68062-2244-1	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
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	68062-2244-1	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
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	68062-2244-1	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
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	68062-2244-1	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
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	68062-2244-1	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
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	68062-2244-1	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	68062-2244-1	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	68062-2244-1	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
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	68062-2244-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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 Advanced Antibacterial Wipes
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	.156 mg/120mg

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 SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
af89bd25-784e-4828-e053-2995a90a8aaa	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68062-2244-1	2025-01-30	C162847	48780-1	2cef2736-599d-d83d-e063-dadaa90ab31f	Dr Lift Advanced Antibacterial Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68062-2244-1	Dr Lift Advanced Antibacterial Wipes	120 mg in 1 BOTTLE	LIQUID	120		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68062-2244	DR LIFT ADVANCED ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE) LIQUID [SPA DE SOLEIL]	1	Current NDC, Legacy NDC, 1 package rows	20200918_af89bd25-784e-4828-e053-2995a90a8aaa.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 57 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Phoenix Healthcare Solutions LLC	e8cdf841-cf56-26cc-e053-2995a90aab51	2025-10-23	Warnings	Exact identifier application number: M003
Povidone Iodine Prep	POVIDONE IODINE	PHOENIX HEALTHCARE SOLUTIONS, LLC	c17603f2-3548-4225-b611-216c2763e51f	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Phoenix Healthcare Solutions LLC	c601d9ea-25ab-cd1d-e053-2995a90ae252	2025-10-23	Warnings	Exact identifier application number: M003
Hand Sanitizer	ALCOHOL	Cardinal Health	cc0a6e1e-ec95-cb48-e053-2a95a90ac0ce	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Phoenix Healthcare Solutions, LLC	d07d103d-420b-5307-e053-2995a90a14f5	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Htl-Strefa, Inc.	d72ddf5a-72e7-c37d-e053-2995a90ad48b	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Phoenix Healthcare Solutions LLC	c92524fd-8b91-592d-e053-2a95a90a88c6	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep	ISOPROPYL ALCOHOL	Cardinal Health	89852887-ae62-4277-b615-75663afb5436	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Henry Schein, Inc.	b9826baa-b976-14c6-e053-2995a90a7d09	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Phoenix Healthcare Solutions LLC	c9261c7f-9f8f-6476-e053-2a95a90a0e93	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pad	ISOPROPYL ALCOHOL	Rugby Laboratories	ea28b27a-456e-4042-b769-f06072759933	2025-10-23	Warnings	Exact identifier application number: M003
School Health Sterile Alcohol Prep Pad	ISOPROPYL ALCOHOL	School Health Corporation	718640e1-826b-4b65-a021-3f82cd4c983a	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Henry Schein, Inc.	215fa8ac-c9b6-42b6-ae9d-a08d7ff0900f	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Cardinal Health	5459a0b4-65ca-455e-80b2-3fe1b24e0137	2025-10-23	Warnings	Exact identifier application number: M003
Hand Sanitizing Wipes	ETHYL ALCOHOL	Phoenix Healthcare Solutions LLC	c68d2d73-be78-8e1c-e053-2995a90a3a37	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep	ISOPROPYL ALCOHOL	PHOENIX HEALTHCARE SOLUTIONS, LLC	a7d77afc-588d-47d7-be2f-686ff3d75da2	2025-10-23	Warnings	Exact identifier application number: M003
Hand Sanitizing Wipes	ETHYL ALCOHOL	PHOENIX HEALTHCARE SOLUTIONS, LLC	ca9f8e68-cc15-42b4-81fd-e114e6a6d7df	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	PHOENIX HEALTHCARE SOLUTIONS, LLC	50b24287-4c91-43d2-9c2e-42d3c086b3b3	2025-10-23	Warnings	Exact identifier application number: M003
Alcohol Prep	ISOPROPYL ALCOHOL	PHOENIX HEALTHCARE SOLUTIONS, LLC	51b707c6-df09-441b-a3d1-3f0c1b0886cc	2025-10-23	Warnings	Exact identifier application number: M003
Povidone Iodine Prep Swabstick	POVIDONE IODINE	PHOENIX HEALTHCARE SOLUTIONS, LLC	8a0aba34-3f96-46b6-8521-f4388fb73edf	2025-10-23	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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68062-2244-1	68062224401	120 mg in 1 BOTTLE (68062-2244-1)	120 mg	2020-09-17	0000-00-00	No	No	Current