Fuzion AB Foam

Product NDC: 66949-111
11-digit product format: 669490111
Labeler code: 66949
Product ID: 66949-111_46de4539-36b3-af75-e063-6294a90acfff
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: LIQUID
Route: TOPICAL
Labeler: Zep Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-03-10
Substance: BENZALKONIUM CHLORIDE
Active strength: .13 g/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Fuzion AB Foam
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	.13 g/100mL

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
b43ea64e-f7db-2250-e053-2995a90a43b3	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66949-111-16	Fuzion AB Foam	4800 mL in 1 CASE	LIQUID	4800		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66949-111	FUZION AB FOAM (BENZALKONIUM CHLORIDE) LIQUID [ZEP INC.]	5	Current NDC, Legacy NDC, 1 package rows	20241120_b43ea64e-f7db-2250-e053-2995a90a43b3.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
Fuzion AB Foam	BENZALKONIUM CHLORIDE	Zep Inc.	b43ea64e-f7db-2250-e053-2995a90a43b3	2025-12-26	Warnings	Exact identifier ndc (product): 66949-111

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	b43ea64e-f7db-2250-e053-2995a90a43b3	6
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	b43ea64e-f7db-2250-e053-2995a90a43b3	6
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	b43ea64e-f7db-2250-e053-2995a90a43b3	6
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	b43ea64e-f7db-2250-e053-2995a90a43b3	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66949-111-16	66949011116	4800 mL in 1 CASE (66949-111-16)	4800 ml	2017-03-10	0000-00-00	No	No	Current