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 structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 68%

OTC - PURPOSE SECTION

Antiseptic

WARNINGS SECTION

Warnings:

For external use only-hands.Flammable.Keep away from heat and flame

OTC - ASK DOCTOR SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

INDICATIONS & USAGE SECTION

Uses：

To decrease bacteria and germs on the skin.
Recommended for repeated use.

DOSAGE & ADMINISTRATION SECTION

Directions:

Wet hands thoroughly with product and allow to dry without wiping.
For children under 6,use only under adult supervision.
Not recommended for infants.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. For children under 6,use only under adult supervision.

OTHER SAFETY INFORMATION

Do not store above 105℉
May discolor some fabrics
Harmful to wood finishes and plastics

INACTIVE INGREDIENT SECTION

Do not store above 105℉
May discolor some fabrics
Harmful to wood finishes and plastics

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236ml236ml

485ml485ml

88ml88ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-222-012022-01-28C16284748780-1d6a99b39-e504-a426-e053-dadaa90af4c247993-222
47993-222-022022-01-28C16284748780-1d6a99b39-e504-a426-e053-dadaa90af4c247993-222
47993-222-032022-01-28C16284748780-1d6a99b39-e504-a426-e053-dadaa90af4c247993-222

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-222-01HAND SANITIZER236 mL in 1 BOTTLE, PUMPGEL2365
47993-222-02HAND SANITIZER485 mL in 1 BOTTLE, PUMPGEL4855
47993-222-03HAND SANITIZER88.7 mL in 1 TUBEGEL88.75

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-222HAND SANITIZER GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]5Legacy NDC, 3 package rows20201105_a2d55815-7578-4718-e053-2a95a90ae8a3.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
47993-22247993-222-01, 47993-222-02, 47993-222-03

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 9404Q93RCW27EIACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
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
b33f0ee8-51d0-5c92-e053-2a95a90a9675a2d55815-7578-4718-e053-2a95a90ae8a32020-11-03WarningsExact identifier
spl id: b33f0ee8-51d0-5c92-e053-2a95a90a9675
spl set id: a2d55815-7578-4718-e053-2a95a90ae8a3

Reported adverse events (FAERS/openFDA)#

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