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
4
Source
full-release
Hydrated at
2026-05-31 23:32:54

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 70%（V/V）

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

INDICATIONS & USAGE SECTION

Uses：

For hand sanitizing to reduce bacteria on the skin.

DOSAGE & ADMINISTRATION SECTION

Directions:

Place enough product in your palm and briskly rub hands together until dry.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water,Carbomer 940,Triethanolamine,Glycerin,Aloe Barbadensis Leaf Juice,Vitamin E

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

237ml237ml

237ml-02237ml-02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-245-012025-01-30C16284748780-12cef2736-7394-d83d-e063-dadaa90ab31f47993-245

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-245-01HAND SANITIZER237 mL in 1 BOTTLEGEL2374

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-245HAND SANITIZER GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]4Legacy NDC, 1 package rows20201105_a447c05a-c7d7-3068-e053-2995a90a0579.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
47993-24547993-245-01

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
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
ALCOHOL3K9958V90MACTIB
TOCOPHEROLR0ZB2556P8IACT
CARBOMER 9404Q93RCW27EIACT

Source Document#

Source XML · Source PDF

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
b343ae8e-9c91-a0b4-e053-2a95a90a7a6da447c05a-c7d7-3068-e053-2995a90a05792020-11-04WarningsExact identifier
spl id: b343ae8e-9c91-a0b4-e053-2a95a90a7a6d
spl set id: a447c05a-c7d7-3068-e053-2995a90a0579

Reported adverse events (FAERS/openFDA)#

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