Hand Sanitizer

Manufacturer
L.E.D. Cosmetics, Inc.
Effective date
2020-05-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:02

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Put a thumbnail size amount in your palm and rub hands briskly until dry. Note: Children under 6 years of age should be supervised during use.

Storage and handling

Do not store above 105°C. May discolor certain fabrics.

Label contents#

Full prescribing information#

Medicinal Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Non-Medicinal:

INACTIVE INGREDIENT SECTION

Water(Aqua), Carbomer, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Parfum.

May Contain:

Yellow 5 Lake (CI 19140), Red 34 (CI 15880), Red 6 Lake (CI 15850), Ferric Ferrocyanide (CI 77510).

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin

Directions:

DOSAGE & ADMINISTRATION SECTION

Put a thumbnail size amount in your palm and rub hands briskly until dry.

Note:

Children under 6 years of age should be supervised during use.

STORAGE AND HANDLING SECTION

Do not store above 105°C. May discolor certain fabrics.

Caution:

WARNINGS SECTION

Flammable. Keep away from fire or flame. For external use only. Keep out of eyes. In case of eye contact, immediately flush with water. If swallowed, call a physician. Discontinue use if irritation or redness develop. If condition persists for more than 72 hours, consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

SPL UNCLASSIFIED SECTION

70% Ethyl Alcohol

Aloe & Vitamin E

Kill 99.9% of Germs

Formulated & developed in USA

Distributed by:

L.E.D Cosmetics Inc.

Diamond Bar, CA, USA. 91765

Made in China

cruelty free Not tested on animals

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77725-001-082022-01-28C16284748780-1d6a99b39-f3e2-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77725-001-08Hand Sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77725-001HAND SANITIZER (ETHYL ALCOHOL) LIQUID [L.E.D. COSMETICS, INC.]1Legacy NDC, 1 package rows20200529_026e7fd4-339c-44fc-ac10-1e8ebcc01ac5.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77725-00177725-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
f6680075-4e9f-4719-8a68-7024a2eecf50026e7fd4-339c-44fc-ac10-1e8ebcc01ac52020-05-26WarningsExact identifier
spl id: f6680075-4e9f-4719-8a68-7024a2eecf50
spl set id: 026e7fd4-339c-44fc-ac10-1e8ebcc01ac5

Reported adverse events (FAERS/openFDA)#

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