Antibacterial Hand Sanitizer

Manufacturer
Aogrand International Trade Corporation
Effective date
2023-02-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:54:00

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Place enough product into your palms and thoroughly spread on both hands rub into skin until dry

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

  • hand Sannitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not apply around eyes. Do not use in ears & mouth.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if redness or irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product into your palms and thoroughly spread on both hands
  • rub into skin until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cocamidopropylamine oxide, C12-20 Alkyl glycoside, glycerin, hydroxyethyl cellulose, Casone (methylisothiazolinone and methylchloroisothiazolinone), citric acid, deionized water

Other information

OTHER SAFETY INFORMATION

  • store below 110F (43C)
  • may discolor certain fabrics or surfaces

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

480g NDC: 74621-006-02

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049228benzalkonium chloride 0.1 % Topical GelPSN4
1049228benzalkonium chloride 0.001 MG/MG Topical GelSCD4
1049228benzalkonium chloride 0.1 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74621-006-02Antibacterial Hand Sanitizer480 g in 1 BOTTLEGEL4804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74621-006ANTIBACTERIAL HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [AOGRAND INTERNATIONAL TRADE CORPORATION]4Legacy NDC, 1 package rows20230213_a60d8d84-4ccf-3cf3-e053-2995a90ad358.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74621-00674621-006-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
f47a1f19-23e9-5f95-e053-2a95a90a093da60d8d84-4ccf-3cf3-e053-2995a90ad3582023-02-11WarningsExact identifier
spl id: f47a1f19-23e9-5f95-e053-2a95a90a093d
spl set id: a60d8d84-4ccf-3cf3-e053-2995a90ad358

Reported adverse events (FAERS/openFDA)#

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