PureForce

Product NDC: 47593-567
Requested package NDC: 47593-567-59
11-digit product format: 475930567
Labeler code: 47593
Product ID: 47593-567_2b024278-ada2-4425-9502-2a6fa4e9e94d
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium chloride
Dosage form: SOLUTION
Route: TOPICAL
Labeler: Ecolab Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-06-14
Substance: BENZALKONIUM CHLORIDE
Active strength: 1 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: PureForce
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
1038791	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
4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
47593-567-30	PureForce	207 mL in 1 BOTTLE, PLASTIC	SOLUTION	207	5
47593-567-41	PureForce	750 mL in 1 BOTTLE, PLASTIC	SOLUTION	750	5
47593-567-59	PureForce	1250 mL in 1 BOTTLE, PLASTIC	SOLUTION	1250	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
47593-567	PUREFORCE (BENZALKONIUM CHLORIDE) SOLUTION [ECOLAB INC.]	4	Current NDC, Legacy NDC, 3 package rows	20240802_4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e.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
PureForce	BENZALKONIUM CHLORIDE	Ecolab Inc.	4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e	2025-12-30	Warnings	Exact identifier ndc (package): 47593-567-59 ndc (product): 47593-567 ndc11 (package): 47593056759

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
1038791	benzalkonium chloride 0.1 % Topical Solution	PSN	4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e	5
1038791	benzalkonium chloride 1 MG/ML Topical Solution	SCD	4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e	5
1038791	benzalkonium chloride 0.1 % Topical Solution	SY	4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
47593-567-59	47593056759	1250 mL in 1 BOTTLE, PLASTIC (47593-567-59)	1250 ml	2016-06-14	0000-00-00	No	No	Current