Antibacterial Hand SanitizerSpray

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
Effective date
2020-11-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:33:01

Label at a glance#

ProductAntibacterial Hand SanitizerSpray
Active ingredientALCOHOL
Label structure9 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:

Flammable: Keep away from high heat or flames.For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - WHEN USING SECTION

keep out of reach of eyes.

DOSAGE & ADMINISTRATION SECTION

Directions:

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis leaf juice.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of hand sanitizer 29mlimage of hand sanitizer 29ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-312-012022-01-28C16284748780-1d6a99b39-9838-a426-e053-dadaa90af4c247993-312

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-312-01Antibacterial Hand SanitizerSpray15 mL in 1 BOTTLE, SPRAYGEL152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-312ANTIBACTERIAL HAND SANITIZERSPRAY (ETHYL ALCOHOL) GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]2Legacy NDC, 1 package rows20201106_4e96ea88-3886-4bc3-8a15-14bec850d900.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47993-31247993-312-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
b366ecbc-77b3-1d83-e053-2995a90a6fb54e96ea88-3886-4bc3-8a15-14bec850d9002020-11-05WarningsExact identifier
spl id: b366ecbc-77b3-1d83-e053-2995a90a6fb5
spl set id: 4e96ea88-3886-4bc3-8a15-14bec850d900

Reported adverse events (FAERS/openFDA)#

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