FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Deviation Distilling LLC
Effective date
2020-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:42

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 80% V/V. PURPOSE: ANTISEPTIC

OTC - PURPOSE SECTION

ANTISEPTIC

DOSAGE & ADMINISTRATION SECTION

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

WARNINGS SECTION

Warnings: For external use only. Flammable. Kepp away from heat or flame.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: glycerin, hydrogen peroxide, purified water USP

INDICATIONS & USAGE SECTION

Use(s): Hand santitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785mL 74105-900-01

Hand Sanitizer Gallon.jpg

GALLONGALLON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236.59 mL 74105-900-08

8OZ8OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3OZ3OZSIZE: 88.72 mL

NDC: 74105-900-03

IMAGE: 3oz bottle label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74105-900-012022-01-28C16284748780-1d6a99b39-bfb3-a426-e053-dadaa90af4c2a1b2673a-51dd-35e4-e053-2a95a90aaeab
74105-900-032022-01-28C16284748780-1d6a99b39-bfb3-a426-e053-dadaa90af4c2a1b2673a-51dd-35e4-e053-2a95a90aaeab
74105-900-082022-01-28C16284748780-1d6a99b39-bfb3-a426-e053-dadaa90af4c2a1b2673a-51dd-35e4-e053-2a95a90aaeab

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74105-900-01Hand Sanitizer3785 mL in 1 BOTTLELIQUID37851
74105-900-03Hand Sanitizer88.72 mL in 1 BOTTLE, SPRAYLIQUID88.721
74105-900-08Hand Sanitizer236.59 mL in 1 BOTTLE, SPRAYLIQUID236.591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74105-900HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [DEVIATION DISTILLING LLC]1Legacy NDC, 3 package rows20200512_a1b2673a-51dd-35e4-e053-2a95a90aaeab.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
74105-90074105-900-01, 74105-900-08, 74105-900-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROGEN PEROXIDEBBX060AN9VIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
a1b2673a-51de-35e4-e053-2a95a90aaeaba1b2673a-51dd-35e4-e053-2a95a90aaeab2020-03-25WarningsExact identifier
spl id: a1b2673a-51de-35e4-e053-2a95a90aaeab
spl set id: a1b2673a-51dd-35e4-e053-2a95a90aaeab

Reported adverse events (FAERS/openFDA)#

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