FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
Effective date
2025-06-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:03:01

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses：

For hand sanitizing to reduce bacteria on the skin.

WARNINGS SECTION

Warnings:

For external use only.

Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Discontinue use if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed，get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water, Glycerin, Carbomer, Fragrance, Triethanolamine, Aloe Barbadensis Leaf Juice, Vitamin E, Iron Oxide（CI77499), Iron Oxide(CI 77492), D&C Red No.30.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of Hand sanitizer 15mlimage of Hand sanitizer 15mlimage of Hand sanitizer 30mlimage of Hand sanitizer 30mlimage of Hand sanitizer 30ml-2image of Hand sanitizer 30ml-2image of Hand sanitizer 30ml-3image of Hand sanitizer 30ml-3image of Hand sanitizer 54mlimage of Hand sanitizer 54ml

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-363-01Hand Sanitizer15 mL in 1 BOTTLEGEL153
47993-363-02Hand Sanitizer30 mL in 1 BOTTLEGEL303
47993-363-03Hand Sanitizer54 mL in 1 BOTTLEGEL543
47993-363-04Hand Sanitizer15 mL in 1 BOTTLEGEL153

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47993-36347993-363-01, 47993-363-02, 47993-363-03, 47993-363-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)132584PQMOIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
D&C RED NO. 302S42T2808BIACT
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
3774025a-a733-8893-e063-6294a90a35f60164027d-0fd7-4b56-acb6-6ba1f094dacf2025-06-13WarningsExact identifier
spl id: 3774025a-a733-8893-e063-6294a90a35f6
spl set id: 0164027d-0fd7-4b56-acb6-6ba1f094dacf

Reported adverse events (FAERS/openFDA)#

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