84641-001 (Antibacterial Hand Sanitizer Spray.)

Manufacturer: NANTONG QINJI HEALTH TECHNOLOGY CO., LTD | NANTONG QINJI HEALTH TECHNOLOGY CO., LTD.
Effective date: 2024-08-19
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 20:56:26

Label at a glance#

ProductAntibacterial Hand Sanitizer Spray.

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

For hand sanitizing to reduce bacteria on the skin.

Dosage and administration

Spray small amount in your palm and briskly rub hands together until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin.

Warinings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire and flame.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes.In case of contact，rinse eyes thoroughly with water.

Discontinue use

OTC - STOP USE SECTION

if irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray small amount in your palm and briskly rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Aloe Barbaensis Leaf Juice.

84641-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84641-001

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Antibacterial Hand Sanitizer Spray.
ALCOHOL
ALOE VERA LEAF
GLYCERIN
PROPYLENE GLYCOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84641-001	84641-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	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
20140312-9e19-4d72-e063-6294a90a4897			1f77e89f-9b71-24cd-e063-6394a90a68a4	2024-08-19	Warnings	Exact identifier spl id: 20140312-9e19-4d72-e063-6294a90a4897 spl set id: 1f77e89f-9b71-24cd-e063-6394a90a68a4

Reported adverse events (FAERS/openFDA)#

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