Hand Sanitizer

Manufacturer
Emerge Technologies, Inc.
Effective date
2020-09-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:27

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping Children under 6 years of age use only under adult supervision Not recommended for infants

Storage and handling

Store below 110F (43C) May discolor fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • on open skin wounds
  • do not inhale or ingest
  • do not use on infants

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water

■Avoid contact with open skin ■ Do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness develops.

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

Wet hands thoroughly with product and allow to dry without wiping
Children under 6 years of age use only under adult supervision
Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

  • Store below 110F (43C)
  • May discolor fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Butylene Glyool, Carbomer, Aminomethyl
Propanol, Aloe Barbadensis Leaf Extract, Xanthan Gum

70 % Alcohol Gel- 1 gallon

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand SanitizerHand Sanitizer

70 % Alcohol Gel-55 gallon

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand SanitizerHand Sanitizer

70 % Alcohol Gel- 275 gallon

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand SanitizerHand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79117-070-012022-01-28C16284748780-1d6a99b39-60e8-a426-e053-dadaa90af4c2Emerge 70 % Alcohol
79117-070-552022-01-28C16284748780-1d6a99b39-60e8-a426-e053-dadaa90af4c2Emerge 70 % Alcohol
79117-070-992022-01-28C16284748780-1d6a99b39-60e8-a426-e053-dadaa90af4c2Emerge 70 % Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79117-070-01Hand Sanitizer3875 mL in 1 JUGGEL38751
79117-070-55Hand Sanitizer208197 mL in 1 DRUMGEL2081971
79117-070-99Hand Sanitizer1040875 mL in 1 DRUMGEL10408751

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79117-070HAND SANITIZER (ALCOHOL) GEL [EMERGE TECHNOLOGIES, INC.]1Legacy NDC, 3 package rows20200916_af642a60-8b31-5acd-e053-2a95a90ae139.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79117-07079117-070-01, 79117-070-55, 79117-070-99

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
af628915-4adb-63ca-e053-2995a90a4440af642a60-8b31-5acd-e053-2a95a90ae1392020-09-15WarningsExact identifier
spl id: af628915-4adb-63ca-e053-2995a90a4440
spl set id: af642a60-8b31-5acd-e053-2a95a90ae139

Reported adverse events (FAERS/openFDA)#

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