Microsure Sanitizer

Manufacturer
Strategia Project Management, Inc.
Effective date
2021-01-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:34

Label at a glance#

ProductMicrosure Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Indications and uses

To help reduce bacteria that potentially cause disease.

Dosage and administration

Wipe sanitizer on target areas for treatment and allow area to dry. Recommended for repeated use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

USES:

INDICATIONS & USAGE SECTION

To help reduce bacteria that potentially cause disease.

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 sanitizer on target areas for treatment and allow area to dry. Recommended for repeated use.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Hydrated Silica Complex

Package Labeling:72513-002-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4mL 72513-002-014mL 72513-002-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72513-002-012023-01-30C16284748780-1f386c649-ca8d-0266-e053-dadaa90a7c1aMicrosure Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72513-002-01Microsure Sanitizer4 mL in 1 POUCHCLOTH41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72513-002MICROSURE SANITIZER (SANITIZING WIPE) CLOTH [STRATEGIA PROJECT MANAGEMENT, INC.]1Legacy NDC, 1 package rows20210130_ba0c63a5-5c4a-986d-e053-2a95a90a0fcb.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72513-00272513-002-01

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ba0c63a5-5c4b-986d-e053-2a95a90a0fcbba0c63a5-5c4a-986d-e053-2a95a90a0fcb2021-01-29WarningsExact identifier
spl id: ba0c63a5-5c4b-986d-e053-2a95a90a0fcb
spl set id: ba0c63a5-5c4a-986d-e053-2a95a90a0fcb

Reported adverse events (FAERS/openFDA)#

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