Hand Sanitizer

Manufacturer
Yiwu Sloggi Cosmetics Co.,ltd | YIWU SLOGGI COSMETICS COLTD
Effective date
2020-06-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:09

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient(s): Ethyl Alcohol 68%

Purpose

OTC - PURPOSE SECTION

Purpose: Antiseptic

Use

INDICATIONS & USAGE SECTION

Rub hands together until dry.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Isopropyl Alcohol

Water

Triethanolamine

Carbomer

Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL NDC: 54225-012-01

30ml label130ml label130ml label230ml label2

100 mL NDC: 54225-012-02

100ml label1100ml label1100ml label2100ml label2

500 mL NDC: 54225-012-03

500ml label1500ml label1500ml label2500ml label2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54225-012-012021-07-23C16284748780-1c7ccaba7-29be-fd44-e053-dadaa90aa01b54225-012
54225-012-022021-07-23C16284748780-1c7ccaba7-29be-fd44-e053-dadaa90aa01b54225-012
54225-012-032021-07-23C16284748780-1c7ccaba7-29be-fd44-e053-dadaa90aa01b54225-012

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54225-012-01Hand Sanitizer30 mL in 1 BOTTLEGEL301
54225-012-02Hand Sanitizer100 mL in 1 BOTTLEGEL1001
54225-012-03Hand Sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54225-012HAND SANITIZER (ETHYL ALCOHOL) GEL [YIWU SLOGGI COSMETICS CO.,LTD]1Legacy NDC, 3 package rows20200605_a73a3365-ea15-d17e-e053-2995a90a8bac.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54225-01254225-012-01, 54225-012-02, 54225-012-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
a73a205a-4504-5583-e053-2a95a90a26eaa73a3365-ea15-d17e-e053-2995a90a8bac2020-06-03WarningsExact identifier
spl id: a73a205a-4504-5583-e053-2a95a90a26ea
spl set id: a73a3365-ea15-d17e-e053-2995a90a8bac

Reported adverse events (FAERS/openFDA)#

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