Hand Sanitizer

Manufacturer
Resource Recovery & Trading LLC
Effective date
2020-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:12

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

to help reduce bacteria on the skin.

Dosage and administration

Apply a small amount in your palm and rub hands together briskly until dry. Children under 6 should be supervised when using this product. Other information Do not store above 110°F (43°C).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame. For external use only.
When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
Stop using and ask doctor if irritation or rash appers 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

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

Children under 6 should be supervised when using this product.

Other information

Do not store above 110°F (43°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, Aloe Barbadensis leaf juice.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77106-001-01Hand Sanitizer60 mL in 1 BOTTLEGEL601
77106-001-02Hand Sanitizer100 mL in 1 BOTTLEGEL1001
77106-001-03Hand Sanitizer200 mL in 1 BOTTLEGEL2001
77106-001-04Hand Sanitizer500 mL in 1 BOTTLEGEL5001
77106-001-05Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
77106-001-06Hand Sanitizer20000 mL in 1 BOTTLEGEL200001
77106-001-07Hand Sanitizer200000 mL in 1 DRUMGEL2000001
77106-001-08Hand Sanitizer1000000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKGEL10000001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77106-001HAND SANITIZER (ALCOHOL) GEL [RESOURCE RECOVERY & TRADING LLC]1Legacy NDC, 8 package rows20200515_bfc2d1bc-19bf-4da3-9cbc-e4a797fc7a69.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
f8b2ef66-6c40-4e74-b806-504fca990bfbbfc2d1bc-19bf-4da3-9cbc-e4a797fc7a692020-05-05WarningsExact identifier
spl id: f8b2ef66-6c40-4e74-b806-504fca990bfb
spl set id: bfc2d1bc-19bf-4da3-9cbc-e4a797fc7a69

Reported adverse events (FAERS/openFDA)#

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