Pure Force

Product NDC: 47593-504
11-digit product format: 475930504
Labeler code: 47593
Product ID: 47593-504_02a396bc-771a-408b-9e39-12631092a9df
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium chloride
Dosage form: LIQUID
Route: TOPICAL
Labeler: Ecolab Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-10-28
Substance: BENZALKONIUM CHLORIDE
Active strength: 1 mg/mL
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	47593-504	47593-504-59	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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Additional Listing Data#

Finished product: Yes
Brand name base: Pure Force
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	1 mg/mL

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
1038799	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
66fd73be-05c8-4905-96f5-f73fa1447b3f	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
47593-504-41	Pure Force	750 mL in 1 BOTTLE, PLASTIC	LIQUID	750		4
47593-504-59	Pure Force	1250 mL in 1 BOTTLE, PLASTIC	LIQUID	1250		4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENZALKONIUM CHLORIDE	ACTIVE INGREDIENT	F5UM2KM3W7	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	1
BENZALKONIUM	ACTIVE MOIETY	7N6JUD5X6Y	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	1
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	1
PROPYLENE	INACTIVE INGREDIENT	AUG1H506LY	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
47593-504	PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]	4	Current NDC, Legacy NDC, 2 package rows	20240711_66fd73be-05c8-4905-96f5-f73fa1447b3f.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
Pure Force	BENZALKONIUM CHLORIDE	Ecolab Inc.	66fd73be-05c8-4905-96f5-f73fa1447b3f	2024-07-09	Warnings	Exact identifier ndc (product): 47593-504

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
1038799	benzalkonium chloride 0.1 % Topical Foam	PSN	66fd73be-05c8-4905-96f5-f73fa1447b3f	4
1038799	benzalkonium chloride 1 MG/ML Topical Foam	SCD	66fd73be-05c8-4905-96f5-f73fa1447b3f	4
1038799	benzalkonium chloride 0.1 % Topical Foam	SY	66fd73be-05c8-4905-96f5-f73fa1447b3f	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
47593-504-41	47593050441	750 mL in 1 BOTTLE, PLASTIC (47593-504-41)	750 ml	2013-10-28	0000-00-00	No	No	Current
47593-504-59	47593050459	1250 mL in 1 BOTTLE, PLASTIC	1250 ml					Historical