FDA.reportPublic FDA data

Antibacterial Hand Sanitizer Spray.

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD | NANTONG QINJI HEALTH TECHNOLOGY CO., LTD
Effective date
2024-08-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:17:25

Label at a glance#

ProductAntibacterial Hand Sanitizer Spray.
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses：

For hand sanitizing to reduce bacteria on the skin.

WARNINGS SECTION

Warnings:

For external use only.

Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Discontinue use 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 right away.

DOSAGE & ADMINISTRATION SECTION

Directions:

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water，Propylene Glycol，Glycerin，Fragrance，Aloe Barbadensis Leaf Juice.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of Antibacterial Hand Sanitizer Spray 20mlimage of Antibacterial Hand Sanitizer Spray 20mlimage of Antibacterial Hand Sanitizer Spray 20ml-2image of Antibacterial Hand Sanitizer Spray 20ml-2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-365-01Antibacterial Hand Sanitizer Spray.20 mL in 1 BOTTLE, SPRAYLIQUID202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-365ANTIBACTERIAL HAND SANITIZER SPRAY. LIQUID [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]21 package rows20240820_af0b96be-d1e2-4d9c-99f3-b58ede34d889.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47993-36547993-365-01

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
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB

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
200207b6-e85e-fd89-e063-6394a90a86cfaf0b96be-d1e2-4d9c-99f3-b58ede34d8892024-08-18WarningsExact identifier
spl id: 200207b6-e85e-fd89-e063-6394a90a86cf
spl set id: af0b96be-d1e2-4d9c-99f3-b58ede34d889

Reported adverse events (FAERS/openFDA)#

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