Instant Hand Antiseptic

Manufacturer
ASP Global | Nantong Health & Beyond Hygienic Products Inc.
Effective date
2024-12-05
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:40:33

Label at a glance#

ProductInstant Hand Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

To help reduce bacteria on hands.

Dosage and administration

Rub dime sized amount between hands until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.095%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on hands.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes and lips. If contact occurs, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub dime sized amount between hands until dry.

Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Methylisothiazolinone, Propylene Glycol, Polyquaternium-37, Triethanolamine. Water

SPL UNCLASSIFIED SECTION

Distributed by :
ASP Global, LLC
7800 Third Flag Parkway,
Austell, GA 30168, USA

PRINCIPAL DISPLAY PANEL - 53 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENGLEWOOD
HEALTH

Instant Hand Antiseptic

Alcohol & Fragrance Free

1.9 FL OZ / 53 mL

Distributed by :
ASP Global, LLC
7800 Third Flag Parkway,
Austell, GA 30168, USA

Rev 03

PRINCIPAL DISPLAY PANEL - 53 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 53 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2048259benzalkonium chloride 0.095 % Topical GelPSN5
2048259benzalkonium chloride 0.00095 MG/MG Topical GelSCD5
2048259benzalkonium chloride 0.095 % Topical GelSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59448-002-01Instant Hand Antiseptic53 mL in 1 BOTTLE, PLASTICGEL535

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59448-002INSTANT HAND ANTISEPTIC (BENZALKONIUM CHLORIDE) GEL [ASP GLOBAL]5Current NDC, Legacy NDC, 1 package rows20241207_4eef4b0f-9209-45a4-8a0e-7891fc380fe5.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59448-00259448-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Englewood Mesh AmenityBENZALKONIUM CHLORIDE AND SODIUM MONOFLUOROPHOSPHATEASP Global, LLca737fe63-6285-41ee-9516-9c3030a0ab482025-12-29WarningsExact identifier
ndc (package): 59448-002-01
ndc11 (package): 59448000201
Englewood AmenityBENZALKONIUM CHLORIDE AND SODIUM MONOFLUOROPHOSPHATEASP Global, LLc7c9ce1bf-6aa2-4073-ad09-2ddf845102a22024-12-17WarningsExact identifier
ndc (package): 59448-002-01
ndc11 (package): 59448000201
Instant Hand AntisepticBENZALKONIUM CHLORIDEASP Global4eef4b0f-9209-45a4-8a0e-7891fc380fe52024-12-05WarningsExact identifier
ndc (package): 59448-002-01
ndc (product): 59448-002
ndc11 (package): 59448000201
spl id: 0fcbb981-7868-4c18-bbfa-10870eb1eadf
spl set id: 4eef4b0f-9209-45a4-8a0e-7891fc380fe5

Reported adverse events (FAERS/openFDA)#

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