Hand Sanitizer

Manufacturer
Oxygen Development, LLC | Oxygen Development LLC
Effective date
2023-02-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:53:57

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Put enough product in your palm to cover hands & rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

USER SAFETY WARNINGS SECTION

For handwashing to decrease bacteria on the skin

When using this product

INDICATIONS & USAGE SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or rash persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands & rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Other Information

OTHER SAFETY INFORMATION

Store below 110 F (43 C). May discolor certain fabric surfaces

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water/Aqua, Glycerin, Fragance, Polysorbate 20, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

61354-018-01_AW61354-018-01_AW

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61354-018-01Hand Sanitizer100 mL in 1 BOTTLELIQUID1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61354-018HAND SANITIZER (ALCOHOL) LIQUID [OXYGEN DEVELOPMENT, LLC]2Legacy NDC, 1 package rows20230211_d423567b-bb89-21fd-e053-2995a90a49f9.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
61354-01861354-018-01

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
f45cc5c4-246f-1c07-e053-2995a90a8244d423567b-bb89-21fd-e053-2995a90a49f92023-02-10WarningsExact identifier
spl id: f45cc5c4-246f-1c07-e053-2995a90a8244
spl set id: d423567b-bb89-21fd-e053-2995a90a49f9

Reported adverse events (FAERS/openFDA)#

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