FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
Effective date
2020-11-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:32:53

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Antiseptic

WARNINGS SECTION

Warnings:

Flammable. Keep away from fire or flame. For external use only. Keep out of reach of children. Keep out of reach of eyes.

INDICATIONS & USAGE SECTION

Uses：

For hand sanitizing to readuce bacteria on the skin.

DOSAGE & ADMINISTRATION SECTION

Directions:

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water,Carbomer 940,Triethanolamine,Glycerin,Aloe Barbadensis,Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

15ml15ml

30ml30ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-238-012025-01-30C16284748780-12cef2736-814a-d83d-e063-dadaa90ab31f47993-238
47993-238-022025-01-30C16284748780-12cef2736-814a-d83d-e063-dadaa90ab31f47993-238

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-238-01HAND SANITIZER15 mL in 1 BOTTLEGEL153
47993-238-02HAND SANITIZER30 mL in 1 BOTTLEGEL303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-238HAND SANITIZER GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]3Legacy NDC, 2 package rows20201105_a3dd4a6c-dc86-d0e4-e053-2995a90ae06e.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
47993-23847993-238-01, 47993-238-02

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
CARBOMER 9404Q93RCW27EIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
GLYCERINPDC6A3C0OXIACT
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
b342bbda-3b94-58cd-e053-2a95a90a7b13a3dd4a6c-dc86-d0e4-e053-2995a90ae06e2020-11-04WarningsExact identifier
spl id: b342bbda-3b94-58cd-e053-2a95a90a7b13
spl set id: a3dd4a6c-dc86-d0e4-e053-2995a90ae06e

Reported adverse events (FAERS/openFDA)#

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