Microsure Hand Sanitizer

Manufacturer: Strategia Project Management, Inc.
Effective date: 2020-12-09
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:34:52

Label at a glance#

ProductMicrosure Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Indications and uses

Sanitizes hands to helps reduce bacteria that potentially cause diseases.

Dosage and administration

Wipe on both hands to disinfect palms, between fingers, back of hands, and wrists. 8 hours of continues protection once skin is fully dry.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

USES:

INDICATIONS & USAGE SECTION

Sanitizes hands to helps reduce bacteria that potentially cause diseases.

WARNINGS:

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

in eyes. If contact occurs, flush thoroughly with water.

Stop use and ask a doctor:

OTC - STOP USE SECTION

If irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Wipe on both hands to disinfect palms, between fingers, back of hands, and wrists. 8 hours of continues protection once skin is fully dry.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Hydrated Silica Complex

Package Labeling:72513-001-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038558	benzalkonium chloride 0.13 % Medicated Pad	PSN	2
1038558	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD	2
1038558	benzalkonium chloride 0.13 % Topical Cloth	SY	2
1038558	benzalkonium chloride 0.13 % Topical Swab	SY	2
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Pad	SY	2
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Swab	SY	2
1038558	benzalkonium chloride 1 ML per 750 ML Topical Swab	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72513-001-00	2022-01-28	C162847	48780-1	d6a99b39-b4ee-a426-e053-dadaa90af4c2	Microsure Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72513-001-00	Microsure Hand Sanitizer	4 mL in 1 PATCH	CLOTH	4		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72513-001	MICROSURE HAND SANITIZER (BENZALKONIUM CHLORIDE) CLOTH [STRATEGIA PROJECT MANAGEMENT, INC.]	2	Legacy NDC, 1 package rows	20201210_ab344569-ef18-9e22-e053-2a95a90a10c0.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Microsure Hand Sanitizer
BENZALKONIUM CHLORIDE
WATER
HYDRATED SILICA
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72513-001	72513-001-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
HYDRATED SILICA	Y6O7T4G8P9	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML

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
b60e51ab-36ba-6863-e053-2995a90a19cf			ab344569-ef18-9e22-e053-2a95a90a10c0	2020-12-09	Warnings	Exact identifier spl id: b60e51ab-36ba-6863-e053-2995a90a19cf spl set id: ab344569-ef18-9e22-e053-2a95a90a10c0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.