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 23:33:05

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 70%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses:

For hand sanitizing to reduce bacteria on the skin.

WARNINGS SECTION

Warnings:

  • Flammable. 
  • Keep away from fire or flame.
  • For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

OTC - WHEN USING SECTION

  • Keep away from eyes.
  • Do not inhale or ingest.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if irritation or redness develops.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Squeeze small amount in your palm and briskly rub hands together, and allow to air dry.
  • For children under 6, use with adult supervision. Not recommended for infants.

OTHER SAFETY INFORMATION

Other information:

  • Store below 110℉(43℃)
  • May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water,Carbomer 940,triethanolamine,Glycerin,Aloe Barbadensis

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of hand sanitizer 237mlimage of hand sanitizer 237ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-278-012025-01-30C16284748780-12cef2736-a1bf-d83d-e063-dadaa90ab31f47993-278

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-278-01HAND SANITIZER237 mL in 1 BOTTLE, PUMPGEL2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-278HAND SANITIZER (ETHYL ALCOHOL) GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]2Legacy NDC, 1 package rows20201106_b82ffb83-25fe-40f6-b453-88ca62b8f71d.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
47993-27847993-278-01

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-8903-0bcc-e053-2a95a90a9c67b82ffb83-25fe-40f6-b453-88ca62b8f71d2020-11-05WarningsExact identifier
spl id: b357014d-8903-0bcc-e053-2a95a90a9c67
spl set id: b82ffb83-25fe-40f6-b453-88ca62b8f71d

Reported adverse events (FAERS/openFDA)#

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