FDA.reportPublic FDA data

HAND SANITIZER

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 23:33:02

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 70%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses：

  • For hand sanitizing to reduce bacteria on the skin. 

WARNINGS SECTION

Warnings:

For external use only - hands.Flammable.

Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Do not inhale or ingest. 

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 

DOSAGE & ADMINISTRATION SECTION

Directions:

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water,Glycerin,Carbomer,Aloe Barbadensis leaf juice,Aminomethyl Propanol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of hand sanitizer 54mlimage of hand sanitizer 54mlimage of hand sanitizer 60mlimage of hand sanitizer 60ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-313-012025-01-30C16284748780-12cef2736-5e4c-d83d-e063-dadaa90ab31f47993-313
47993-313-022025-01-30C16284748780-12cef2736-5e4c-d83d-e063-dadaa90ab31f47993-313

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-313-01HAND SANITIZER54 mL in 1 BOTTLEGEL542
47993-313-02HAND SANITIZER60 mL in 1 BOTTLEGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-313HAND SANITIZER GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]2Legacy NDC, 2 package rows20201106_6e2764cc-0127-4d98-8ed5-2b5b982aa8e3.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47993-31347993-313-01, 47993-313-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
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
b367b1b1-8563-638d-e053-2995a90a1e876e2764cc-0127-4d98-8ed5-2b5b982aa8e32020-11-05WarningsExact identifier
spl id: b367b1b1-8563-638d-e053-2995a90a1e87
spl set id: 6e2764cc-0127-4d98-8ed5-2b5b982aa8e3

Reported adverse events (FAERS/openFDA)#

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