8HD Hand and Skin Sanitizer

Manufacturer
Strategia Project Management, Inc.
Effective date
2023-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:05:15

Label at a glance#

Product8HD Hand and Skin Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

Sanitizes hands and skin to help reduce bacteria that potentially cause diseases.

Dosage and administration

On dry hands, place enough product in your palms to thoroughly cover the targeted area. Rub briskly until entirely 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 and skin to help 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

On dry hands, place enough product in your palms to thoroughly cover the targeted area. Rub briskly until entirely dry.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Hydrated Silica Complex

Package Labeling:72513-200-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1oz 72513-200-011oz 72513-200-01

Package Labeling:72513-200-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2oz 72513-200-022oz 72513-200-02

Package Labeling:72513-200-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1L 72513-200-031L 72513-200-03

Package Labeling:72513-200-04

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1Gal 72513-200-041Gal 72513-200-04

Package Labeling:72513-200-05

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

55Gal 72513-200-0555Gal 72513-200-05

Package Labeling:72513-200-06

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

275Gal 72513-200-06275Gal 72513-200-06

Package Labeling:72513-200-07

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

330Gal 72513-200-07330Gal 72513-200-07

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN2
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD2
1049254benzalkonium chloride 0.13 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72513-200-018HD Hand and Skin Sanitizer29.57 mL in 1 BOTTLELIQUID29.572
72513-200-028HD Hand and Skin Sanitizer59.14 mL in 1 BOTTLELIQUID59.142
72513-200-038HD Hand and Skin Sanitizer1000 mL in 1 BOTTLELIQUID10002
72513-200-048HD Hand and Skin Sanitizer3785.41 mL in 1 JUGLIQUID3785.412
72513-200-058HD Hand and Skin Sanitizer208198 mL in 1 DRUMLIQUID2081982
72513-200-068HD Hand and Skin Sanitizer1040988.2 mL in 1 CONTAINERLIQUID1040988.22
72513-200-078HD Hand and Skin Sanitizer1249185.9 mL in 1 CONTAINERLIQUID1249185.92

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72513-2008HD HAND AND SKIN SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [STRATEGIA PROJECT MANAGEMENT, INC.]2Legacy NDC, 7 package rows20231221_b68a4cf8-0214-7dad-e053-2a95a90a04f5.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72513-20072513-200-01, 72513-200-02, 72513-200-03, 72513-200-04, 72513-200-05, 72513-200-06, 72513-200-07

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
0cf46e3d-9b2b-c091-e063-6394a90aa8adb68a4cf8-0214-7dad-e053-2a95a90a04f52023-12-20WarningsExact identifier
spl id: 0cf46e3d-9b2b-c091-e063-6394a90aa8ad
spl set id: b68a4cf8-0214-7dad-e053-2a95a90a04f5

Reported adverse events (FAERS/openFDA)#

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