Hand Protector

Manufacturer
Cytonix, LLC | Elaine Lanza
Effective date
2020-09-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:29:30

Label at a glance#

ProductHand Protector
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose: Antiseptic. Hand and skin sanitizer.

INDICATIONS & USAGE SECTION

USES: to reduce bacteria on skin that could cause disease. Recommended for repeat use.

WARNINGS SECTION

WARNINGS

For external use only.
Do not use in eyes.
When using this product avoid contact with eyes. In case of eye contact flush with water. Stop use and ask doctor if irritation and redness develop.
Keep out of reach of children.
If swallowed, get medical attention or contact a Poison Control Center.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of eye contact flush with plenty of water.

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or redness develop.

INACTIVE INGREDIENT SECTION

3-(trimethoxysilyl) Propyl Dimethyl Octadecyl Ammonium Chloride, Ethyl Alcohol, Water

DOSAGE & ADMINISTRATION SECTION

Apply liberally to hands and gently rub until dry. Reapply after 4 hours.

OTC - QUESTIONS SECTION

Contact:

Cytonix LLC, Beltsville, MD

20705 USA 301-470-6267

www.cytonix.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Protector label 79291-653-03 16oz (473mL)

Hand Protector label 79291-653-03 16oz(473mL)Hand Protector label 79291-653-03 16oz(473mL)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN3
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD3
1049254benzalkonium chloride 0.13 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79291-653-01Hand Protector120 mL in 1 BOTTLE, DISPENSINGSOLUTION1203
79291-653-02Hand Protector473 mL in 1 BOTTLE, SPRAYSOLUTION4733
79291-653-03Hand Protector473 mL in 1 BOTTLE, SPRAYSOLUTION4733

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79291-653HAND PROTECTOR (BENZALKONIUM CHLORIDE) SOLUTION [CYTONIX, LLC]3Legacy NDC, 3 package rows20200917_a8d482d1-2925-107f-e053-2995a90ab812.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79291-65379291-653-01, 79291-653-02, 79291-653-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
af618f60-7d29-a21d-e053-2995a90a1c9ba8d482d1-2925-107f-e053-2995a90ab8122020-09-15WarningsExact identifier
spl id: af618f60-7d29-a21d-e053-2995a90a1c9b
spl set id: a8d482d1-2925-107f-e053-2995a90ab812

Reported adverse events (FAERS/openFDA)#

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