Emely Hand Sanitizer (Gel)

Manufacturer
Laboratorios E&M SRL
Effective date
2021-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:11

Label at a glance#

ProductEmely Hand Sanitizer
Active ingredientALCOHOL
Label structure17 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

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

Alcohol 80% v/v Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Aseptic, Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

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.

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.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

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

Glicerin, Purified Water USP, Triethanolamine, Carbomer

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​60 mL NDC: 77998-001-10 60 mL Gel60 mL Gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

120 mL NDC: 77998-001-20

120 mL Gel120 mL Gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

240 mL NDC: 77998-001-30

240 mL Gel240 mL Gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

480 mL NDC: 77998-001-40

480 mL Gel480 mL Gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

960 mL NDC: 77998-001-50

960 mL Gel960 mL Gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1920 mL NDC: 77998-001-60

1920 mL Gel1920 mL Gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785 mL NDC: 77998-001-70

3785 mL Gel3785 mL Gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN2
1041498ethanol 0.8 ML/ML Topical GelSCD2
1041498ethanol 80 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77998-001-10Emely Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL602
77998-001-20Emely Hand Sanitizer120 mL in 1 BOTTLE, PLASTICGEL1202
77998-001-30Emely Hand Sanitizer240 mL in 1 BOTTLE, PLASTICGEL2402
77998-001-40Emely Hand Sanitizer480 mL in 1 BOTTLE, PLASTICGEL4802
77998-001-50Emely Hand Sanitizer960 mL in 1 BOTTLE, PLASTICGEL9602
77998-001-60Emely Hand Sanitizer1920 mL in 1 BOTTLE, PLASTICGEL19202
77998-001-70Emely Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICGEL37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77998-001EMELY HAND SANITIZER (ALCOHOL) GEL [LABORATORIOS E&M SRL]2Legacy NDC, 7 package rows20220101_a62ad6dc-d0a4-581f-e053-2995a90a469a.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
77998-00177998-001-10, 77998-001-20, 77998-001-30, 77998-001-40, 77998-001-50, 77998-001-60, 77998-001-70

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
d46e541d-7a0a-6eda-e053-2a95a90ac820a62ad6dc-d0a4-581f-e053-2995a90a469a2021-12-31WarningsExact identifier
spl id: d46e541d-7a0a-6eda-e053-2a95a90ac820
spl set id: a62ad6dc-d0a4-581f-e053-2995a90a469a

Reported adverse events (FAERS/openFDA)#

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