Hand Sanitizer

Manufacturer
ZHEJIANG STELCO CHEMICALS CO. LTD
Effective date
2020-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:48

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product onto your palm and rub handstogether briskly until dry. Children under 6 years of ages hould be supervised when using this product.

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

Ethyl Alcohol 70% v/v....Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

WARNING SFLAMMABLE. KEEP AWAY FROM FIRE OR FLAMEFOR EXTERNAL USE ONLY

Do not use

OTC - DO NOT USE SECTION

DO NOT USE this product in or near the eyes. In case ofeye contact, flush with plenty of water.

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

Stop use and consult 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product onto your palm and rub handstogether briskly until dry. Children under 6 years of ages hould be supervised when using this product.

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

Water(Aqua), Propylene Glycol, Glycerin, C10-30 AlkylAcrylate Crosspolymer, Triethanolamine, Vitamin E, Fragrance( Parfum)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11223344

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75705-005-01Hand Sanitizer30 mL in 1 BOTTLEGEL301
75705-005-02Hand Sanitizer60 mL in 1 BOTTLEGEL601
75705-005-03Hand Sanitizer236 mL in 1 BOTTLEGEL2361
75705-005-04Hand Sanitizer354 mL in 1 BOTTLEGEL3541

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75705-005HAND SANITIZER GEL [ZHEJIANG STELCO CHEMICALS CO. LTD]1Legacy NDC, 4 package rows20200506_a4e560ac-65c4-222f-e053-2a95a90a08c1.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
75705-00575705-005-01, 75705-005-02, 75705-005-03, 75705-005-04

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
a4e39218-981c-1d81-e053-2995a90afce3a4e560ac-65c4-222f-e053-2a95a90a08c12020-05-05WarningsExact identifier
spl id: a4e39218-981c-1d81-e053-2995a90afce3
spl set id: a4e560ac-65c4-222f-e053-2a95a90a08c1

Reported adverse events (FAERS/openFDA)#

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