ProCure Foaming Antimicrobial Hand

Product NDC: 55681-042
11-digit product format: 556810042
Labeler code: 55681
Product ID: 55681-042_3e002cee-6103-1db4-e063-6394a90ac7a1
Type: HUMAN OTC DRUG
Nonproprietary name: Hand Soap (Benzalkonium Chloride 0.13%)
Dosage form: SOAP
Route: TOPICAL
Labeler: Twin Med LLC
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-09-04
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: ProCure Foaming Antimicrobial Hand
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
3e002cee-6102-1db4-e063-6394a90ac7a1	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55681-042-10	ProCure Foaming Antimicrobial Hand	1000 mL in 1 CARTRIDGE	SOAP	1000		1

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
ProCure Foaming Antimicrobial Hand	HAND SOAP (BENZALKONIUM CHLORIDE 0.13%)	Twin Med LLC	3e002cee-6102-1db4-e063-6394a90ac7a1	2025-09-04	Warnings	Exact identifier ndc (product): 55681-042

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	3e002cee-6102-1db4-e063-6394a90ac7a1	1
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	3e002cee-6102-1db4-e063-6394a90ac7a1	1
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	3e002cee-6102-1db4-e063-6394a90ac7a1	1
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	3e002cee-6102-1db4-e063-6394a90ac7a1	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
55681-042-10	55681004210	1000 mL in 1 CARTRIDGE (55681-042-10)	1000 ml	2025-09-04	No	No	Current