Dr Lift Antibacterial Body Scrub

Product NDC: 68062-2240
11-digit product format: 680622240
Labeler code: 68062
Product ID: 68062-2240_50b7202c-ebc3-d203-e063-6394a90ac911
Type: HUMAN OTC DRUG
Nonproprietary name: benzalkonium chloride
Dosage form: GEL
Route: TOPICAL
Labeler: Spa de Soleil
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-07-29
Substance: BENZALKONIUM CHLORIDE
Active strength: .23 mg/180mg
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	68062-2240-1	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	68062-2240-1	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	68062-2240-1	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	68062-2240-1	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	68062-2240-1	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	68062-2240-1	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	68062-2240-1	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	68062-2240-1	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	68062-2240-1	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 Body Scrub
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	.23 mg/180mg

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
ab9d6c73-29c1-036a-e053-2995a90a449c	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68062-2240-1	2025-01-30	C162847	48780-1	2cef2736-6b42-d83d-e063-dadaa90ab31f	Dr Lift Antibacterial Body Scrub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68062-2240-1	Dr Lift Antibacterial Body Scrub	180 mg in 1 TUBE	GEL	180		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68062-2240	DR LIFT ANTIBACTERIAL BODY SCRUB (BENZALKONIUM CHLORIDE) GEL [SPA DE SOLEIL]	1	Current NDC, Legacy NDC, 1 package rows	20200730_ab9d6c73-29c1-036a-e053-2995a90a449c.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 34 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Topco Associates LLC	be4f41bd-8a75-4fb6-8d28-67f6f853e6bd	2026-02-11	Warnings, Adverse reactions	Exact identifier application number: M003
70% Isopropyl Rubbing Alcohol	ISOPROPYL RUBBING ALCOHOL	Topco Associates LLC	9fbded5f-8dc1-4134-a711-48d1a581d874	2026-02-11	Warnings, Adverse reactions	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Topco Associates LLC	ad1ef2ea-bfc3-4a8a-acd2-55e7f52813d4	2026-02-11	Warnings, Adverse reactions	Exact identifier application number: M003
Antibacterial Wet wipes	BENZALKONIUM CHLORIDE	Zhejiang Easyclean Daily Chemical Co., Ltd.	a1cb6ac9-95f5-3ef1-e053-2a95a90abcdf	2026-02-11	Warnings	Exact identifier application number: M003
Universal ISOPROPYL Rubbing Alcohol 70%	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	0c76f14b-9a0c-4573-96f2-cd4080eb99e6	2026-02-10	Warnings	Exact identifier application number: M003
Ethyl Rubbing Alcohol	ETHYL ALCOHOL	Walgreen Co.	a08ef11f-5c4f-4821-a0c0-d6c89def0bea	2026-02-10	Warnings, Adverse reactions	Exact identifier application number: M003
70%	ISOPROPYL ALCOHOL	Walgreen Co.	fb918e7a-1fe0-4cfd-8cf0-9d823eb56dcc	2026-02-10	Warnings, Adverse reactions	Exact identifier application number: M003
AMERICAN RED CROSS ANTISEPTIC CLEANSING FOAM	BENZALKONIUM CL 0.13% V/V	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	49e31509-d489-44be-e063-6394a90a97ef	2026-02-10	Warnings	Exact identifier application number: M003
AMERICAN RED CROSS ANTISEPTIC CLEANSING FOAM	BENZALKONIUM CL 0.13% V/V	MY IMPORTS USA LLC	4a849c4f-9b96-6b20-e063-6394a90a3486	2026-02-10	Warnings	Exact identifier application number: M003
Medline	ISOPROPYL ALCOHOL	Hy-Vee, Inc.	4bbce274-1e62-0c6a-e063-6394a90af92f	2026-02-10	Warnings	Exact identifier application number: M003
Everlit Care Products Antiseptic Wipe	ANTISEPTIC WIPE	EVERLIT GLOBAL INC.	3331e2f1-c3d0-41fc-a792-be5dcdf4e24a	2026-02-09	Warnings	Exact identifier application number: M003
EVERLIT CARE PRODUCTS PREP PAD	ISOPROPYL ALCOHOL	EVERLIT GLOBAL INC.	77a60360-8bb5-43e9-b7e4-f71d2d488c44	2026-02-09	Warnings	Exact identifier application number: M003
Everlit Care Products Sting Relief	ISOPROPYL ALCOHOL	EVERLIT GLOBAL INC.	adfab206-b7de-4f6a-a864-edd946ea743d	2026-02-09	Warnings	Exact identifier application number: M003
EVERLIT CARE PRODUCTS IODINE PREP PAD	POVIDONE-IODINE	EVERLIT GLOBAL INC.	5cbdb73d-333a-4244-a1c0-be430632f0ed	2026-02-09	Warnings	Exact identifier application number: M003
Alcohol	ISOPROPYL ALCOHOL	A-S Medication Solutions	6b8834be-0235-4f7c-8d52-c2f6aa2d3049	2026-02-08	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Salado Sales Inc.	78a46975-568a-4a88-8597-9603b8bbf935	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M003
70% Rubbing	ISOPROPYL ALCOHOL	Walgreens Co.	6ad37d18-5c19-4b5f-8313-edd430f84fb0	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Walgreens Co.	1473e6e4-dc5f-43d9-a249-111a181e3f76	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M003
Aquarrelle Antibacterial Wipes 40	BENZALKONIUM CHLORIDE	Kimberly-Clark De Mexico, S.A.B.deC.V.	3584680e-71b0-23b6-e063-6294a90a6998	2026-02-05	Warnings	Exact identifier application number: M003
Aquarrelle Antibacterial Wipes 20	BENZALKONIUM CHLORIDE	Kimberly-Clark De Mexico, S.A.B.deC.V.	35865d33-a99f-1b37-e063-6394a90a00d2	2026-02-05	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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68062-2240-1	68062224001	180 mg in 1 TUBE (68062-2240-1)	180 mg	2020-07-29	0000-00-00	No	No	Current