All Day Hand Sanitizer

Manufacturer: BPI Packaging, LLC
Effective date: 2020-06-25
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:19:12

Label at a glance#

ProductAll Day Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure11 sections

Dosage and administration

Directioins: Apply liberally to the hands and gently rub ubtil dry

Label contents#

Full prescribing information#

Active Ingredient Purpose

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%...Antimicrobial

OTC - PURPOSE SECTION

Antimicrobial

Dosage and Administration

INDICATIONS & USAGE SECTION

Directioins: Apply liberally to the hands and gently rub ubtil dry

Warnings

WARNINGS SECTION

For External use Only.

OTC - WHEN USING SECTION

When Using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Pioson Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to the hands and gently rub until dry.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

1-Octadecanaminium N, N Dimethyl-N-(3(Trihydroxysilyl) Propyl) Chloride, Water

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TEKO Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79039-300-26	2021-07-23	C162847	48780-1	c7ccaba7-173d-fd44-e053-dadaa90aa01b	a84f1699-b652-bf0c-e053-2a95a90a2ed4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79039-300-26	All Day Hand Sanitizer	3800 mL in 1 JUG	LIQUID	3800		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79039-300	ALL DAY HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [BPI PACKAGING, LLC]	2	Legacy NDC, 1 package rows	20200627_a84f1699-b652-bf0c-e053-2a95a90a2ed4.zip

Products#

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

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

All Day Hand Sanitizer
Benzalkonium Chloride
BENZALKONIUM
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79039-300	79039-300-26

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
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT

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
a8efa851-e1e3-6739-e053-2a95a90a1d6b			a84f1699-b652-bf0c-e053-2a95a90a2ed4	2020-06-25	Warnings	Exact identifier spl id: a8efa851-e1e3-6739-e053-2a95a90a1d6b spl set id: a84f1699-b652-bf0c-e053-2a95a90a2ed4

Reported adverse events (FAERS/openFDA)#

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