ProCure Foaming Hand Sanitizer

Product NDC: 55681-040
11-digit product format: 556810040
Labeler code: 55681
Product ID: 55681-040_3d848ec8-5198-6d39-e063-6394a90aaef6
Type: HUMAN OTC DRUG
Nonproprietary name: Ethyl Alcohol 72%
Dosage form: GEL
Route: TOPICAL
Labeler: Twin Med LLC
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-09-01
Substance: ALCOHOL
Active strength: 72 mL/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 Hand Sanitizer
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	72 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2277550	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
3d848ec8-5197-6d39-e063-6394a90aaef6	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55681-040-10	ProCure Foaming Hand Sanitizer	1000 mL in 1 CARTRIDGE	GEL	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 Hand Sanitizer	ETHYL ALCOHOL 72%	Twin Med LLC	3d848ec8-5197-6d39-e063-6394a90aaef6	2026-05-29	Warnings	Exact identifier ndc (product): 55681-040

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2277550	ethanol 72 % Topical Gel	PSN	3d848ec8-5197-6d39-e063-6394a90aaef6	2
2277550	ethanol 0.72 ML/ML Topical Gel	SCD	3d848ec8-5197-6d39-e063-6394a90aaef6	2
2277550	ethanol 72 % Topical Gel	SY	3d848ec8-5197-6d39-e063-6394a90aaef6	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
55681-040-10	55681004010	1000 mL in 1 CARTRIDGE (55681-040-10)	1000 ml	2025-09-01	No	No	Current