HAND SANITIZER

Manufacturer
INGBO JIANGBEI OCEAN STAR TRADING CO.,LTD | 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 structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Alcohol 71% v/v

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses:

Hand sanitizer to help reduce germs on the skin that potentially can cause disease.

WARNINGS SECTION

Warnings:

Flammable. Keep away from fire or flame

For external use only.

OTC - STOP USE SECTION

Discontinue use and ask a doctor if

  • Irritation and redness develop.
  • Condition persists for more than 72 hours.

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Spray on clean, dry hands and nails.
  • Wet hands thoroughly with product.
  • Rub hands together for no less than 15 seconds, paying particular attention to interdigital spaces, fingernails and cuticles.
  • Allow to dry without wiping.
  • Rub hands together briskly until dry.

OTHER SAFETY INFORMATION

Other information:

Store in a cool, dry place below 104℉ (40℃).

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2282911ethanol 71 % Topical GelPSN1
2282911ethanol 0.71 ML/ML Topical GelSCD1
2282911ethanol 71 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130044600021744GTIN-13: 0044600021744
EAN-13: 0044600021744
GTIN-12: 044600021744
UPC-A: 044600021744
GTIN storage (14 digits): 00044600021744
59ml.jpg
BarcodeEAN-130044600021768GTIN-13: 0044600021768
EAN-13: 0044600021768
GTIN-12: 044600021768
UPC-A: 044600021768
GTIN storage (14 digits): 00044600021768
500ml.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-329-012025-01-30C16284748780-12cef2736-889b-d83d-e063-dadaa90ab31f47993-329
47993-329-022025-01-30C16284748780-12cef2736-889b-d83d-e063-dadaa90ab31f47993-329

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-329-01HAND SANITIZER59 mL in 1 BOTTLE, SPRAYGEL591
47993-329-02HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-329HAND SANITIZER (ETHYL ALCOHOL) GEL [INGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]1Legacy NDC, 2 package rows20210617_c1535db8-80cf-40d4-b367-a71091b6b1c4.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
47993-32947993-329-01, 47993-329-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
c4f14922-709c-59c6-e053-2995a90a065ec1535db8-80cf-40d4-b367-a71091b6b1c42021-06-17WarningsExact identifier
spl id: c4f14922-709c-59c6-e053-2995a90a065e
spl set id: c1535db8-80cf-40d4-b367-a71091b6b1c4

Reported adverse events (FAERS/openFDA)#

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