QBlue Hand Sanitizer Solution 1000mL (83388-002-10)

Manufacturer
QBLUE TECHNOLOGIES, INC.
Effective date
2023-04-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:54:41

Label at a glance#

ProductHAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Dosage and administration

Spray onto hands or skin and apply evenly until dry. Do not dilute. Use as directed.

Storage and handling

Store at room temperature. Avoid direct sunlight. Do not refrigerate. Use within 9 months after opening

Label contents#

Full prescribing information#

Drug Facts - Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.09%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, rinse eye thoroughly with water.

Do not Use

OTC - DO NOT USE SECTION

on open skin wounds.

Stop Use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray onto hands or skin and apply evenly until dry.
  • Do not dilute. Use as directed.

Other Information

STORAGE AND HANDLING SECTION

  • Store at room temperature. Avoid direct sunlight.
  • Do not refrigerate.
  • Use within 9 months after opening

Inactive Ingredients

INACTIVE INGREDIENT SECTION

titanium dioxide, purified water

Questions or comment?

OTC - QUESTIONS SECTION

1-833-387-9949

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 83388-002-10

Alcohol-free non-allergenic water-based sanitizing solution. Kills and blocks 99.9% of all germs. Made without parabens, sulfates, phthalates, fragrances or dyes. Gentle and safe for children, pets, elders, and the environment.

Science-based
Pure Ingredients
Net WT: 5 fl.oz (150 mL)
Reuse and
recycle
Made in Hong Kong, China.
US patent no. 17049546
Distributed By
QBlue Technologies, Inc.
4521 PGA Blvd STE 510
Palm Bch Gardens, FL 33418

labelabe

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2634304benzalkonium chloride 0.09 % Topical SprayPSN2
2634304benzalkonium chloride 0.9 MG/ML Topical SpraySCD2
2634304benzalkonium chloride 0.09 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83388-002-10HAND SANITIZER1000 mL in 1 POUCHSOLUTION10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83388-002HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [QBLUE TECHNOLOGIES, INC.]21 package rows20230411_f902f66d-dfac-3365-e053-6394a90a6d71.zip

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
83388-00283388-002-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
f9039552-11da-a4a3-e053-6294a90a9049f902f66d-dfac-3365-e053-6394a90a6d712023-04-10WarningsExact identifier
spl id: f9039552-11da-a4a3-e053-6294a90a9049
spl set id: f902f66d-dfac-3365-e053-6394a90a6d71

Reported adverse events (FAERS/openFDA)#

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