FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
Effective date
2020-10-29
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:32:33

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure8 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:

Flammable: Keep away from fire or flame.For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Keep out of reach of eyes.

DOSAGE & ADMINISTRATION SECTION

Directions:

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

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water，Carbomer ，Triethanolamine，Glycerin，Aloe Barbadensis leaf juice

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

237ml237ml

500ml500ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-214-012022-01-28C16284748780-1d6a99b39-cb9b-a426-e053-dadaa90af4c247993-214
47993-214-022022-01-28C16284748780-1d6a99b39-cb9b-a426-e053-dadaa90af4c247993-214
47993-214-032022-01-28C16284748780-1d6a99b39-cb9b-a426-e053-dadaa90af4c247993-214

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-214-01HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5005
47993-214-02HAND SANITIZER237 mL in 1 BOTTLE, PUMPGEL2375
47993-214-03HAND SANITIZER237 mL in 1 BOTTLEGEL2375

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-214HAND SANITIZER GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]5Legacy NDC, 3 package rows20201029_a1a84757-6b8b-c3ac-e053-2a95a90ad797.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
47993-21447993-214-01, 47993-214-02, 47993-214-03

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
CARBOMER 9404Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
b2cb3fad-a9fa-f79d-e053-2a95a90ad691a1a84757-6b8b-c3ac-e053-2a95a90ad7972020-10-29WarningsExact identifier
spl id: b2cb3fad-a9fa-f79d-e053-2a95a90ad691
spl set id: a1a84757-6b8b-c3ac-e053-2a95a90ad797

Reported adverse events (FAERS/openFDA)#

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