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 23:32:56

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%

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water,Carbomer,Triethanolamine,Glycerol and Aloe Vera Extract.

INDICATIONS & USAGE SECTION

Uses：

Hand sanitizer to decrease bacteria on the skin.

DOSAGE & ADMINISTRATION SECTION

Apply small amount and rub hands together until dry.

WARNINGS SECTION

Warnings:

Do not use in the eyes. In case of contact, rise eyes with water. Stop use and ask a doctor if irritation and redness develop and last for more than

72 hours. Get medical help immediately if swallowed. 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.

OTC - PURPOSE SECTION

Antiseptic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

237ml237ml

500ml500ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-261-012022-01-28C16284748780-1d6a99b39-7e64-a426-e053-dadaa90af4c247993-261
47993-261-022022-01-28C16284748780-1d6a99b39-7e64-a426-e053-dadaa90af4c247993-261
47993-261-032022-01-28C16284748780-1d6a99b39-7e64-a426-e053-dadaa90af4c247993-261

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-261-01HAND SANITIZER237 mL in 1 BOTTLE, PUMPGEL2373
47993-261-02HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5003
47993-261-03HAND SANITIZER60 mL in 1 BOTTLEGEL603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-261HAND SANITIZER GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]3Legacy NDC, 3 package rows20201105_a5a9eb0c-5abd-125a-e053-2995a90a97b8.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
47993-26147993-261-01, 47993-261-02, 47993-261-03

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
CARBOMER 9404Q93RCW27EIACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT

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
b346e070-d642-aeab-e053-2995a90a8a01a5a9eb0c-5abd-125a-e053-2995a90a97b82020-11-04WarningsExact identifier
spl id: b346e070-d642-aeab-e053-2995a90a8a01
spl set id: a5a9eb0c-5abd-125a-e053-2995a90a97b8

Reported adverse events (FAERS/openFDA)#

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