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 23:33:06

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:

  • Hand Sanitizer to help reduce bacteria 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 eyes 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. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Put enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

OTHER SAFETY INFORMATION

Other information:

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

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water,Glycerin,Carbomer,Aloe Barbadensis Leaf Juice,Aminomethyl Propanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of hand sanitizer 60mlimage of hand sanitizer 60mlimage of hand sanitizer 100mlimage of hand sanitizer 100mlimage of hand sanitizer 237mlimage of hand sanitizer 237mlimage of hand sanitizer 3785mlimage of hand sanitizer 3785mlimage of hand sanitizer 1000mlimage of hand sanitizer 1000ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47993-318-012022-01-28C16284748780-1d6a99b39-9856-a426-e053-dadaa90af4c247993-318
47993-318-022022-01-28C16284748780-1d6a99b39-9856-a426-e053-dadaa90af4c247993-318
47993-318-032022-01-28C16284748780-1d6a99b39-9856-a426-e053-dadaa90af4c247993-318
47993-318-042022-01-28C16284748780-1d6a99b39-9856-a426-e053-dadaa90af4c247993-318
47993-318-052022-01-28C16284748780-1d6a99b39-9856-a426-e053-dadaa90af4c247993-318

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47993-318-01HAND SANITIZER60 mL in 1 BOTTLEGEL602
47993-318-02HAND SANITIZER100 mL in 1 BOTTLEGEL1002
47993-318-03HAND SANITIZER237 mL in 1 BOTTLEGEL2372
47993-318-04HAND SANITIZER1000 mL in 1 BOTTLEGEL10002
47993-318-05HAND SANITIZER3785 mL in 1 BOTTLE, PUMPGEL37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47993-318HAND SANITIZER (ETHYL ALCOHOL) GEL [NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD]2Legacy NDC, 5 package rows20201106_bdf111d8-a41b-4f37-a00d-2219ea48db3f.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
47993-31847993-318-01, 47993-318-02, 47993-318-03, 47993-318-04, 47993-318-05

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
b3681014-b87a-638f-e053-2995a90a533dbdf111d8-a41b-4f37-a00d-2219ea48db3f2020-11-05WarningsExact identifier
spl id: b3681014-b87a-638f-e053-2995a90a533d
spl set id: bdf111d8-a41b-4f37-a00d-2219ea48db3f

Reported adverse events (FAERS/openFDA)#

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