Hand Sanitizer (Rinse-free)

Manufacturer
Shanghai Rayshine ENVI-TECH Developing CO., Ltd.
Effective date
2020-05-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:13:22

Label at a glance#

ProductHand Sanitizer (Rinse-free)
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand sanitizing to reduce bacteria on the skin.

Dosage and administration

Squeez small amount in your palm and briskly rub hands together until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION


Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION


Antiseptic

Uses

INDICATIONS & USAGE SECTION


For hand sanitizing to reduce bacteria
on the skin.

Warnings

WARNINGS SECTION


For extermal use only-hands. Flamable.Keep awaysfrom fire and flame.

When using this product

OTC - WHEN USING SECTION


Keep out of eyes.Do not inhale or ingest. Stop use and ask a doctor if skinimitation develops. Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION


Squeez small amount in your palm and briskly rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION


Water,Carbomer,Triethanolamine,Glycerin,Vitamin E,Aloe Barbadensis.Fragrance.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 ml label30 ml label50 ml label50 ml label54 ml label54 ml label60 ml label60 ml label80 ml label80 ml label90 ml label90 ml label100 ml label100 ml label250 ml label250 ml label500 ml label500 ml label1000 ml label1000 ml label2000 ml label2000 ml label3785 ml label3785 ml label5000 ml label5000 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75129-001-01Hand Sanitizer (Rinse-free)30 mL in 1 BOTTLEGEL302
75129-001-02Hand Sanitizer (Rinse-free)50 mL in 1 BOTTLEGEL502
75129-001-03Hand Sanitizer (Rinse-free)54 mL in 1 BOTTLEGEL542
75129-001-04Hand Sanitizer (Rinse-free)60 mL in 1 BOTTLEGEL602
75129-001-05Hand Sanitizer (Rinse-free)80 mL in 1 BOTTLEGEL802
75129-001-06Hand Sanitizer (Rinse-free)90 mL in 1 BOTTLEGEL902
75129-001-07Hand Sanitizer (Rinse-free)100 mL in 1 BOTTLEGEL1002
75129-001-08Hand Sanitizer (Rinse-free)250 mL in 1 BOTTLEGEL2502
75129-001-09Hand Sanitizer (Rinse-free)500 mL in 1 BOTTLEGEL5002
75129-001-10Hand Sanitizer (Rinse-free)1000 mL in 1 BOTTLEGEL10002
75129-001-11Hand Sanitizer (Rinse-free)2000 mL in 1 BOTTLEGEL20002
75129-001-12Hand Sanitizer (Rinse-free)3785 mL in 1 BOTTLEGEL37852
75129-001-13Hand Sanitizer (Rinse-free)5000 mL in 1 BOTTLEGEL50002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75129-001HAND SANITIZER (RINSE-FREE) GEL [SHANGHAI RAYSHINE ENVI-TECH DEVELOPING CO., LTD.]2Legacy NDC, 13 package rows20200518_a3886f94-1862-6910-e053-2995a90a1056.zip

Products#

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

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

NDC Codes#

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
a5e31ae9-e366-4313-e053-2995a90a32caa3886f94-1862-6910-e053-2995a90a10562020-05-17WarningsExact identifier
spl id: a5e31ae9-e366-4313-e053-2995a90a32ca
spl set id: a3886f94-1862-6910-e053-2995a90a1056

Reported adverse events (FAERS/openFDA)#

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