FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
Effective date
2020-11-03
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:32:51

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 reduce bacteria on the skin.

DOSAGE & ADMINISTRATION SECTION

Directions:

Pump out small amount 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,Triethanolamine,Glycerin,Aloe Barbadensis leaf juice,Vitamin E

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50ml50ml

237ml237ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-219-012022-01-28C16284748780-1d6a99b39-7df8-a426-e053-dadaa90af4c247993-219
47993-219-022022-01-28C16284748780-1d6a99b39-7df8-a426-e053-dadaa90af4c247993-219

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-219-01HAND SANITIZER50 mL in 1 BOTTLEGEL505
47993-219-02HAND SANITIZER237 mL in 1 BOTTLEGEL2375

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-219HAND SANITIZER GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]5Legacy NDC, 2 package rows20201105_a25a1030-e9ea-345f-e053-2a95a90a7ea0.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
47993-21947993-219-01, 47993-219-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
TOCOPHEROLR0ZB2556P8IACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
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
b33eb226-8156-d5f9-e053-2a95a90a26eba25a1030-e9ea-345f-e053-2a95a90a7ea02020-11-03WarningsExact identifier
spl id: b33eb226-8156-d5f9-e053-2a95a90a26eb
spl set id: a25a1030-e9ea-345f-e053-2a95a90a7ea0

Reported adverse events (FAERS/openFDA)#

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