FDA.reportPublic FDA data

Hand Santizer

Manufacturer
Robert Mazza, Inc dba Five & 20 Spirits | Robert Mazza, Inc.
Effective date
2020-04-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:05:08

Label at a glance#

ProductHand Santizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

For topical use only

OTC - ACTIVE INGREDIENT SECTION

Alcohol - 80%ABV

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Water

INDICATIONS & USAGE SECTION

For external use only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

OTC - PURPOSE SECTION

Sanitizer - for hands

WARNINGS SECTION

For external use only, flammable, keep away from heat or flame.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN2
1039339ethanol 0.8 ML/ML Topical SolutionSCD2
1039339ethanol 80 % Topical SolutionSY2

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
74054-100-022022-01-28C16284748780-1d6a99b39-5498-a426-e053-dadaa90af4c2a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-032022-01-28C16284748780-1d6a99b39-5498-a426-e053-dadaa90af4c2a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-042022-01-28C16284748780-1d6a99b39-5498-a426-e053-dadaa90af4c2a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-052022-01-28C16284748780-1d6a99b39-5498-a426-e053-dadaa90af4c2a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-062022-01-28C16284748780-1d6a99b39-5498-a426-e053-dadaa90af4c2a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-072022-01-28C16284748780-1d6a99b39-5498-a426-e053-dadaa90af4c2a268e759-9a3f-1d7b-e053-2a95a90a335b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74054-100-02Hand Santizer118 mL in 1 BOTTLE, PLASTICLIQUID1182
74054-100-03Hand Santizer237 mL in 1 BOTTLE, PLASTICLIQUID2372
74054-100-04Hand Santizer3785 mL in 1 BOTTLE, PLASTICLIQUID37852
74054-100-05Hand Santizer18927 mL in 1 BOTTLE, PLASTICLIQUID189272
74054-100-06Hand Santizer355 mL in 1 BOTTLE, PLASTICLIQUID3552
74054-100-07Hand Santizer473 mL in 1 BOTTLE, PLASTICLIQUID4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74054-100HAND SANTIZER (ALCOHOL) LIQUID [ROBERT MAZZA, INC DBA FIVE & 20 SPIRITS]2Legacy NDC, 6 package rows20200407_a268e759-9a3f-1d7b-e053-2a95a90a335b.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
74054-10074054-100-02, 74054-100-03, 74054-100-04, 74054-100-05, 74054-100-06, 74054-100-07

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
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT

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
a26931b6-3ab9-3356-e053-2995a90a1959a268e759-9a3f-1d7b-e053-2a95a90a335b2020-04-03WarningsExact identifier
spl id: a26931b6-3ab9-3356-e053-2995a90a1959
spl set id: a268e759-9a3f-1d7b-e053-2a95a90a335b

Reported adverse events (FAERS/openFDA)#

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