FDA.reportPublic FDA data

Secure Instant Foaming Hand Sanitizer

Manufacturer
American Cleaning Solutions
Effective date
2009-10-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:54:34

Label at a glance#

ProductSecure Instant Foaming Hand Sanitizer
Active ingredientBenzalkonium Chloride
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                          Purpose

Benzalkonium Chloride 0.1%............Antimicrobial

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

WARNINGS SECTION

Warnings

For external use only.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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.

DOSAGE & ADMINISTRATION SECTION

Directions

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 INGREDIENT SECTION

Inactive ingredients

Water, dihydroxypropyl PEG-5, linoleammonium chloride, glycereth-2 cocoate, behetrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Secure Instant Foaming Hand Sanitizer

solutions plus

Alcohol Free

Kills 99.9% of most common germs that make you sick.

128 Fl oz. (3.85 Liters)

container labelcontainer label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49922-001-012025-12-06C16284748780-1956f9ecf-d8b1-621f-e053-dbdaa90a74adDrug Facts
49922-001-022025-12-06C16284748780-1956f9ecf-d8b1-621f-e053-dbdaa90a74adDrug Facts
49922-001-032025-12-06C16284748780-1956f9ecf-d8b1-621f-e053-dbdaa90a74adDrug Facts
49922-001-012019-10-21C16284748780-1956f9ecf-d8b1-621f-e053-dbdaa90a74adDrug Facts
49922-001-022019-10-21C16284748780-1956f9ecf-d8b1-621f-e053-dbdaa90a74adDrug Facts
49922-001-032019-10-21C16284748780-1956f9ecf-d8b1-621f-e053-dbdaa90a74adDrug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49922-001SECURE INSTANT FOAMING HAND SANITIZER (HAND SANITIZER) LIQUID [AMERICAN CLEANING SOLUTIONS]1Legacy NDC20091209_295d73ce-0f31-4789-9a00-5f8ff25f9920.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y1
WaterINACTIVE INGREDIENT059QF0KO0R1

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
49922-00149922-001-01, 49922-001-02, 49922-001-03

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
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT

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
ef0a810b-b64d-4b73-a2de-b9b5ead22de5295d73ce-0f31-4789-9a00-5f8ff25f99202025-11-15WarningsExact identifier
spl set id: 295d73ce-0f31-4789-9a00-5f8ff25f9920

Reported adverse events (FAERS/openFDA)#

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