Refresh AntiBac FOAM

Product NDC: 11084-010
11-digit product format: 110840010
Labeler code: 11084
Product ID: 11084-010_eb4c478c-f612-4163-9145-59d414bc8273
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: SOAP
Route: TOPICAL
Labeler: SC Johnson Professional USA Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-06-12
Substance: BENZALKONIUM CHLORIDE
Active strength: .13 g/L
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 · 5 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	11084-010	11084-010-01	D	Discontinued by firm	2026-08-11
excluded package	package	11084-010	11084-010-27	D	Discontinued by firm	2026-08-11
excluded package	package	11084-010	11084-010-40	D	Discontinued by firm	2026-08-11
excluded package	package	11084-010	11084-010-55	D	Discontinued by firm	2026-08-11
excluded package	package	11084-010	11084-010-96	D	Discontinued by firm	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 1 · 36 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	11084-010-55	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11084-010-40	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11084-010-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11084-010-96	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	11084-010-55	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11084-010-40	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11084-010-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11084-010-96	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	11084-010-55	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11084-010-40	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11084-010-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11084-010-96	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	11084-010-55	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11084-010-40	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11084-010-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11084-010-96	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	11084-010-55	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11084-010-40	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11084-010-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11084-010-96	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	11084-010-55	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11084-010-40	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11084-010-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11084-010-96	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	11084-010-55	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11084-010-40	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11084-010-01	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11084-010-96	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	11084-010-55	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	11084-010-40	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	11084-010-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	11084-010-96	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	11084-010-55	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	11084-010-40	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	11084-010-01	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	11084-010-96	`0efc9e666f02…`	`f202fb6c5f17…`

Additional Listing Data#

Finished product: Yes
Brand name base: Refresh AntiBac FOAM
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	.13 g/L

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
1046593	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
884d1c8c-5643-423e-8ed4-d2ef38f8af73	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11084-010-01	Refresh AntiBac FOAM	0.047 L in 1 BOTTLE, PLASTIC	SOAP	0.047	10
11084-010-05	Refresh AntiBac FOAM	3.78 L in 1 BOTTLE, PLASTIC	SOAP	3.78	10
11084-010-12	Refresh AntiBac FOAM	1.2 L in 1 BOTTLE, PLASTIC	SOAP	1.2	10
11084-010-20	Refresh AntiBac FOAM	2 L in 1 BOTTLE, PLASTIC	SOAP	2	10
11084-010-27	Refresh AntiBac FOAM	1 L in 1 BOTTLE, PLASTIC	SOAP	1	10
11084-010-40	Refresh AntiBac FOAM	0.4 L in 1 BOTTLE, PLASTIC	SOAP	0.4	10
11084-010-55	Refresh AntiBac FOAM	208.2 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK	SOAP	208.2	10
11084-010-66	Refresh AntiBac FOAM	1 L in 1 BOTTLE, PLASTIC	SOAP	1	10
11084-010-96	Refresh AntiBac FOAM	0.296 L in 1 BOTTLE, PLASTIC	SOAP	0.296	10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11084-010	REFRESH ANTIBAC FOAM (BENZALKONIUM CHLORIDE) SOAP [SC JOHNSON PROFESSIONAL USA, INC.]	7	Current NDC, Legacy NDC, 9 package rows	20241220_884d1c8c-5643-423e-8ed4-d2ef38f8af73.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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Refresh AntiBac FOAM	BENZALKONIUM CHLORIDE	SC Johnson Professional USA Inc.	884d1c8c-5643-423e-8ed4-d2ef38f8af73	2025-12-23	Warnings	Exact identifier ndc (product): 11084-010

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
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	884d1c8c-5643-423e-8ed4-d2ef38f8af73	10
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	884d1c8c-5643-423e-8ed4-d2ef38f8af73	10
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	884d1c8c-5643-423e-8ed4-d2ef38f8af73	10
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	884d1c8c-5643-423e-8ed4-d2ef38f8af73	10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11084-010-01	11084001001	.047 L in 1 BOTTLE, PLASTIC (11084-010-01)		2019-02-27	0000-00-00	Yes	No	Current
11084-010-05	11084001005	3.78 L in 1 BOTTLE, PLASTIC (11084-010-05)	3.78 l	2017-06-12	0000-00-00	No	No	Current
11084-010-12	11084001012	1.2 L in 1 BOTTLE, PLASTIC (11084-010-12)	1.2 l	2017-06-12	0000-00-00	No	No	Current
11084-010-20	11084001020	2 L in 1 BOTTLE, PLASTIC (11084-010-20)	2 l	2017-06-12	0000-00-00	No	No	Current
11084-010-27	11084001027	1 L in 1 BOTTLE, PLASTIC (11084-010-27)	1 l	2017-06-12	0000-00-00	No	No	Current
11084-010-40	11084001040	.4 L in 1 BOTTLE, PLASTIC (11084-010-40)		2017-06-12	0000-00-00	No	No	Current
11084-010-55	11084001055	208.2 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (11084-010-55)	208.2 l	2019-02-27	0000-00-00	Yes	No	Current
11084-010-66	11084001066	1 L in 1 BOTTLE, PLASTIC (11084-010-66)	1 l	2022-12-31	0000-00-00	No	No	Current
11084-010-96	11084001096	.296 L in 1 BOTTLE, PLASTIC (11084-010-96)		2019-08-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	SC Johnson Professional USA Inc. \| APEX International, Inc.	2025-12-23	HUMAN OTC DRUG LABEL	10