Foaming Hand Sanitizer

Manufacturer: Specialty Water Resources, Llc
Effective date: 2020-07-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:22:29

Label at a glance#

ProductFoaming Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

• For hand sanitizing to decrease bacteria on the skin • Recommended for repeated use

Dosage and administration

• Pump a small amount of foam into palm of hand • Rub thoroughly over all surfaces of both hands • Rub hands together briskly until dry

Contacts and useful links#

PhoneLabel contact1-877-377-9687

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Pump a small amount of foam into palm of hand
• Rub thoroughly over all surfaces of both hands
• Rub hands together briskly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, d-glucopyranose, oligomeric, decyl octyl glycosides, glycerol, methylisothiazolinone, and citric acid.

SPL UNCLASSIFIED SECTION

For Your Water

"What is your mission?"

no alcohol

dye and fragrance free

soft on skin with moisturizers

MUST BE USED WITH FOAMING DISPENSER / PUMP

MADE IN THE USA

WARNING

KEEP OUT OF REACH OF CHILDREN.

MAY BE HARMFUL IF SWALLOWED.

MAY CAUSE EYE IRRITATION.

SEE BACK PANEL FOR ADDITIONAL PRECAUTIONS AND FIRST AID.

INSTITUTIONAL & COMMERCIAL HAND SANITIZER

Before discarding container, rinse with water.

For institutional and commercial use.

MFG For: For Your Water

11804 Woodruff Ave., Downey, CA 90241

Ph: 1-877-377-9687

For Additional Product and Safety Information
See Safety Data Sheet

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79724-375-81	2022-01-28	C162847	48780-1	d6a99b39-abd4-a426-e053-dadaa90af4c2	For Your Water Foaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79724-375-81	Foaming Hand Sanitizer	3780 mL in 1 BOTTLE	LIQUID	3780		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79724-375	FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SPECIALTY WATER RESOURCES, LLC]	1	Legacy NDC, 1 package rows	20200725_45560ef5-ca83-4c09-bc24-d08f7fa1e863.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Foaming Hand Sanitizer
Benzalkonium Chloride
BENZALKONIUM
WATER
2,3 DI-O-METHYL-D-GLUCOSE
CAPRYL OLIGOGLUCOSIDE
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE
GLYCERIN
METHYLISOTHIAZOLINONE
CITRIC ACID MONOHYDRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79724-375	79724-375-81

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
2,3 DI-O-METHYL-D-GLUCOSE	3F1Y194PDX	IACT
CAPRYL OLIGOGLUCOSIDE	VXR09E583M	IACT
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE	E00JL9G9K0	IACT
GLYCERIN	PDC6A3C0OX	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	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
ab1226c7-59e3-4b55-82cf-e961825177ba			45560ef5-ca83-4c09-bc24-d08f7fa1e863	2020-07-23	Warnings	Exact identifier spl id: ab1226c7-59e3-4b55-82cf-e961825177ba spl set id: 45560ef5-ca83-4c09-bc24-d08f7fa1e863

Reported adverse events (FAERS/openFDA)#

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