HAND SANITIZER

Manufacturer
NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
Effective date
2020-11-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:33:00

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl alcohol 62%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses:

Hand sanitizer to help reduce bacteria on the skin.

WARNINGS SECTION

Warnings:

Flammable. keep away from heat and flame. For external use only.

OTC - WHEN USING SECTION

When using this product.

Keep out of eyes. Do not inhale or ingest. Stop use and ask a doctor if skin irritation develops. Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions:

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500ml-1500ml-1

500ml-2500ml-2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-280-012022-01-28C16284748780-1d6a99b39-e5a4-a426-e053-dadaa90af4c247993-280

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-280-01HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-280HAND SANITIZER (ETHYL ALCOHOL) GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]2Legacy NDC, 1 package rows20201106_26d6101f-2a9b-42b1-9981-c65d405e07b9.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
47993-28047993-280-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
b357014d-8905-0bcc-e053-2a95a90a9c6726d6101f-2a9b-42b1-9981-c65d405e07b92020-11-05WarningsExact identifier
spl id: b357014d-8905-0bcc-e053-2a95a90a9c67
spl set id: 26d6101f-2a9b-42b1-9981-c65d405e07b9

Reported adverse events (FAERS/openFDA)#

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