FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
Effective date
2021-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:51

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethanol Alcohol 71% v/v

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses：

Hand sanitizer to help reduce germs on the skin.

WARNINGS SECTION

Warnings:

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes, In case of contact, rinse thoroughly with water.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

If swallowed, get medical help or contact a Poison Control Center Immediately.

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Glycerin, Propylene Glycol, Fragrance, Aloe Barbedensis Leaf Juice, Tocopherol Acetate (VITAMIN E)

OTHER SAFETY INFORMATION

Other information:

Store below 106℉(41℃).

May discolor certain fabrics.

DOSAGE & ADMINISTRATION SECTION

Directions:

Spray product into palms and rub together until dry. Adult supervision is recommended for children under age 6.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of Paper card 1image of Paper card 1image of Paper card 2image of Paper card 2image of hand sanitizer 29.87mlimage of hand sanitizer 29.87ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1665370ethanol 71 % Topical SolutionPSN1
1665370ethanol 0.71 ML/ML Topical SolutionSCD1
1665370ethanol 71 % Topical SolutionSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130742797857022GTIN-13: 0742797857022
EAN-13: 0742797857022
GTIN-12: 742797857022
UPC-A: 742797857022
GTIN storage (14 digits): 00742797857022		Paper card 1.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-328-012025-01-30C16284748780-12cef2736-6c10-d83d-e063-dadaa90ab31f47993-328

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-328-01HAND SANITIZER29.87 mL in 1 BOTTLE, SPRAYLIQUID29.871

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-328HAND SANITIZER (ETHYL ALCOHOL) LIQUID [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]1Legacy NDC, 1 package rows20210617_954a3a55-3487-4e2a-8a13-3a179ddc5726.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
47993-32847993-328-01

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
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
c4f14cb7-3da9-2272-e053-2995a90ab24f954a3a55-3487-4e2a-8a13-3a179ddc57262021-06-17WarningsExact identifier
spl id: c4f14cb7-3da9-2272-e053-2995a90ab24f
spl set id: 954a3a55-3487-4e2a-8a13-3a179ddc5726

Reported adverse events (FAERS/openFDA)#

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