QBlue Hand Sanitizer Solution 50mL (83388-003-50)

Manufacturer: QBLUE TECHNOLOGIES, INC.
Effective date: 2023-04-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:54:41

Label at a glance#

ProductANTIBACTERIAL SANITIZING AND MOISTURIZING HAND

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

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

Dosage and administration

Apply product thoroughly to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed.

Storage and handling

Avoid direct sunlight. Store below 50°C. Do not refrigerate.

Contacts and useful links#

PhoneLabel contact1-833-387-9949

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

Avoid contact with eyes.

OTC - WHEN USING SECTION

In case of contact, rinse eyes thoroughly with water.

Do not Use

OTC - DO NOT USE SECTION

on open skin wounds.

If irritation develops

OTC - STOP USE SECTION

Discontinue use and consult a doctor.

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

Apply product thoroughly to hands.
Rub hands together until absorbed.
Do not wipe off or rinse. Apply to
hands as needed.

Other Information

STORAGE AND HANDLING SECTION

Avoid direct sunlight. Store below
50°C. Do not refrigerate.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Mineral Oil, Glyceryl
Stearate, Stearic Acid, Fragrance,
Cetearyl Alcohol, Acrylates /C10-30
Alkyl Acrylate, Glycerin, Sodium
Hydroxide, Crosspolymer, Vitamin B,
Vitamin E, Titanium Dioxide.

Questions or comment?

OTC - QUESTIONS SECTION

1-833-387-9949

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 83388-001-15

box

label

label 2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2634305	benzalkonium chloride 0.09 % Topical Cream	PSN	1
2634305	benzalkonium chloride 0.9 MG/ML Topical Cream	SCD	1
2634305	benzalkonium chloride 0.09 % Topical Cream	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
83388-003-50	2024-07-30	C162847	48780-1	1030e365-2887-111a-e063-dadaa90a10e2	QBlue Hand Sanitizer Solution 50mL (83388-003-50)
83388-003-50	2024-01-30	C162847	48780-1	1030e365-2887-111a-e063-dadaa90a10e2	QBlue Hand Sanitizer Solution 50mL (83388-003-50)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83388-003-50	ANTIBACTERIAL SANITIZING AND MOISTURIZING HAND	50 mL in 1 CONTAINER	CREAM	50		1
83388-003-50	ANTIBACTERIAL SANITIZING AND MOISTURIZING HAND	1 in 1 BOX	CREAM	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83388-003	ANTIBACTERIAL SANITIZING AND MOISTURIZING HAND (BENZALKONIUM CHLORIDE) CREAM [QBLUE TECHNOLOGIES, INC.]	1	2 package rows	20230411_f90340a1-7dc8-34b5-e053-6294a90ae3b7.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

ANTIBACTERIAL SANITIZING AND MOISTURIZING HAND
BENZALKONIUM CHLORIDE
CETOSTEARYL ALCOHOL
GLYCERIN
SODIUM HYDROXIDE
.ALPHA.-TOCOPHEROL
TITANIUM DIOXIDE
GLYCERYL STEARATE SE
STEARIC ACID
MINERAL OIL
BENZALKONIUM
WATER
CARBOMER COPOLYMER TYPE A

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83388-003	83388-003-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
GLYCERYL STEARATE SE	FCZ5MH785I	IACT
STEARIC ACID	4ELV7Z65AP	IACT
MINERAL OIL	T5L8T28FGP	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
CARBOMER COPOLYMER TYPE A	71DD5V995L	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
f90335c1-7fd9-bd3d-e053-6394a90ac9b8			f90340a1-7dc8-34b5-e053-6294a90ae3b7	2023-04-10	Warnings	Exact identifier spl id: f90335c1-7fd9-bd3d-e053-6394a90ac9b8 spl set id: f90340a1-7dc8-34b5-e053-6294a90ae3b7

Reported adverse events (FAERS/openFDA)#

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