Sani-Foam Foaming Non-Alcohol Hand Sanitizer

Product NDC: 62767-104
Requested package NDC: 62767-104-39
11-digit product format: 627670104
Labeler code: 62767
Product ID: 62767-104_41d9312a-863e-6139-e063-6294a90ae1bf
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: SOLUTION
Route: TOPICAL
Labeler: Multi-Clean
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-01-17
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: Sani-Foam Foaming Non-Alcohol Hand Sanitizer
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
2bea7ec7-e79e-8f34-e063-6294a90a9609	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
62767-104-31	Sani-Foam Foaming Non-Alcohol Hand Sanitizer	50 mL in 1 BOTTLE, PUMP	SOLUTION	50	2
62767-104-33	Sani-Foam Foaming Non-Alcohol Hand Sanitizer	3785 mL in 1 BOTTLE, PLASTIC	SOLUTION	3785	2
62767-104-37	Sani-Foam Foaming Non-Alcohol Hand Sanitizer	208198 mL in 1 DRUM	SOLUTION	208198	2
62767-104-39	Sani-Foam Foaming Non-Alcohol Hand Sanitizer	50 mL in 1 BOTTLE, PUMP	SOLUTION	50	2
62767-104-39	Sani-Foam Foaming Non-Alcohol Hand Sanitizer	24 in 1 BOX	SOLUTION	24	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62767-104	SANI-FOAM FOAMING NON-ALCOHOL HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [MULTI-CLEAN]	1	Current NDC, 5 package rows	20250119_2bea7ec7-e79e-8f34-e063-6294a90a9609.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
Sani-Foam Foaming Non-Alcohol Hand Sanitizer	BENZALKONIUM CHLORIDE	Multi-Clean	2bea7ec7-e79e-8f34-e063-6294a90a9609	2025-10-23	Warnings	Exact identifier ndc (package): 62767-104-39 ndc (product): 62767-104 ndc11 (package): 62767010439

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	2bea7ec7-e79e-8f34-e063-6294a90a9609	2
1038799	benzalkonium chloride 1 MG/ML Topical Foam	SCD	2bea7ec7-e79e-8f34-e063-6294a90a9609	2
1038799	benzalkonium chloride 0.1 % Topical Foam	SY	2bea7ec7-e79e-8f34-e063-6294a90a9609	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Sample	Exclude flag	Status
62767-104-39	62767010439	24 BOTTLE, PUMP in 1 BOX (62767-104-39) / 50 mL in 1 BOTTLE, PUMP	2025-10-23	No	No	Current