Dr Lift Antibacterial

Product NDC: 68062-2243
11-digit product format: 680622243
Labeler code: 68062
Product ID: 68062-2243_40d7c6af-e655-d3e5-e063-6394a90af01c
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: LOTION
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: 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 · 16 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
2025-08-27 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	68062-2243-1	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	68062-2243-1	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	68062-2243-1	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	68062-2243-1	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	68062-2243-1	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	68062-2243-1	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	68062-2243-1	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	68062-2243-1	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 Antibacterial
Listing expiration: 2026-12-31

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 RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1046442	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
af89675e-e66f-0922-e053-2995a90ab9d2	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68062-2243-1	2025-01-30	C162847	48780-1	2cef2736-89bd-d83d-e063-dadaa90ab31f	Dr Lift Antibacterial Body Lotion
68062-2243-1	2025-01-30	C162847	48780-1	2cef2736-89bd-d83d-e063-dadaa90ab31f	Dr Lift Antibacterial Body Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68062-2243-1	Dr Lift Antibacterial	120 mg in 1 BOTTLE	LOTION	120		2
68062-2243-2	Dr Lift Antibacterial	100 mg in 1 BOTTLE	LOTION	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68062-2243	DR LIFT ANTIBACTERIAL (BENZALKONIUM CHLORIDE) LOTION [SPA DE SOLEIL]	1	Current NDC, Legacy NDC, 2 package rows	20200918_af89675e-e66f-0922-e053-2995a90ab9d2.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 29 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens Sanitizing Wipes	WALGREENS SANITIZING WIPES	Walgreens	42de3b25-692b-eaff-e063-6294a90a0d21	2026-03-11	Warnings	Exact identifier application number: M003
70% Isopropyl Alcohol	ISOPROPYL ALCOHOL	Amazon.com Services LLC	106f51fa-e687-470f-8ed8-35cb0565aeff	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Amazon.com Services LLC	4ab76d25-136d-45e2-b9d7-964777e1d855	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Perrigo Direct, Inc	2efcda54-b8b7-4266-89c0-7f686c7afdca	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M003
Alcohol Antiseptic Pads	ISOPROPYL ALCOHOL	Acme United Corporation	4cc307b9-aee2-3ce0-e063-6294a90aa169	2026-03-11	Warnings	Exact identifier application number: M003
Isopropyl alcohol	ISOPROPYL ALCOHOL	Salado Sales Inc.	30294cad-d806-4d5b-8c86-484f22d214b6	2026-03-10	Warnings, Adverse reactions	Exact identifier application number: M003
mild iodine tincture	IODINE AND SODIUM IODINE AND ALCOHOL	KROGER COMPANY	42762471-e5cb-505e-e063-6294a90afb7d	2026-03-10	Warnings	Exact identifier application number: M003
Numstat Antiseptic and Pain-Relieving Prep Pad	ANTISEPTIC AND PAIN-RELIEVING PREP PAD	Safetec of America Inc.	4c9c20f2-bc17-857b-e063-6394a90a5d5c	2026-03-09	Warnings	Exact identifier application number: M003
Eco Bandage OCEAN	BENZETHONIUM CHLORIDE	ECO Bandage LLC	c7867df0-e167-4ec6-921b-6a0fb3cb0614	2026-03-06	Warnings	Exact identifier application number: M003
Eco Bandage HONEY	BENZETHONIUM CHLORIDE	Eco Bandage LLC	d2faa027-b274-43c0-9b87-85efab89fe8e	2026-03-06	Warnings	Exact identifier application number: M003
Eco Bandage HIBISCUS	BENZETHONIUM CHLORIDE	Eco Bandage LLC	41f8716d-a970-40cd-a29d-69dafc97def8	2026-03-06	Warnings	Exact identifier application number: M003
Eco Bandage MOCHA	BENZETHONIUM CHLORIDE	Eco Bandage LLC	11ec42e4-49d1-4690-80c3-784f2e30acd3	2026-03-06	Warnings	Exact identifier application number: M003
Eco Bandage SAND	BENZETHONIUM CHLORIDE	Eco Bandage LLC	5c620696-e8eb-445e-b746-5348ea37a214	2026-03-06	Warnings	Exact identifier application number: M003
Eco Bandage sand ocean	BENZETHONIUM CHLORIDE	Eco Bandage LLC	da0c2d07-bc2a-4e7c-af45-f921375b52e1	2026-03-06	Warnings	Exact identifier application number: M003
MediChoice Antiseptic Isopropyl Alcohol Prep Pads	ISOPROPYL ALCOHOL	O&M HALYARD, INC.	20b3694e-04c7-4bca-b2ce-62ae0dec7a83	2026-03-05	Warnings	Exact identifier application number: M003
MediChoice Alcohol Swabstick	ISOPROPYL ALCOHOL	O&M HALYARD, INC.	7f78529d-df17-44b3-a890-1afa35308c67	2026-03-05	Warnings	Exact identifier application number: M003
MediChoice Alcohol Prep Pads	ISOPROPYL ALCOHOL	O&M HALYARD, INC.	f4f54448-0de0-448c-9b7b-104370953ae5	2026-03-05	Warnings	Exact identifier application number: M003
MediChoice Alcohol Swabstick	ISOPROPYL ALCOHOL	O&M HALYARD, INC.	7cee1141-4a49-4fec-a627-91a88e3d3ffc	2026-03-05	Warnings	Exact identifier application number: M003
Loris BZK Antiseptic Wipes	BENZALKONIUM CHLORIDE	LernaPharm Loris Inc.	a448de7b-4d96-4d53-ae1a-0bd38a2fb4a2	2026-03-05	Warnings	Exact identifier application number: M003
SPA HAND SANITIZER WRTER MELON SPLASH	ETHYL ALCOHOL	Rejoice International Corp.	4c53620d-01ee-8ddd-e063-6294a90a8a2b	2026-03-05	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
1046442	benzalkonium chloride 0.13 % Topical Lotion	PSN	af89675e-e66f-0922-e053-2995a90ab9d2	2
1046442	benzalkonium chloride 1.3 MG/ML Topical Lotion	SCD	af89675e-e66f-0922-e053-2995a90ab9d2	2
1046442	benzalkonium chloride 0.13 % Topical Lotion	SY	af89675e-e66f-0922-e053-2995a90ab9d2	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68062-2243-1	68062224301	120 mg in 1 BOTTLE (68062-2243-1)	120 mg	2020-09-17	0000-00-00	No	No	Current
68062-2243-2	68062224302	100 mg in 1 BOTTLE (68062-2243-2)	100 mg	2025-10-10		No	No	Current