FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
LiDestri Beverages, LLC
Effective date
2020-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:12

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3780 ml Mandarin3780 ml Mandarin

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75539-003-032022-01-28C16284748780-1d6a99b39-f60d-a426-e053-dadaa90af4c2a85c4933-62ae-ccd9-e053-2a95a90a364b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75539-003-03Hand Sanitizer3780 mL in 1 BOTTLESOLUTION37801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75539-003HAND SANITIZER (ALCOHOL) SOLUTION [LIDESTRI BEVERAGES, LLC]1Legacy NDC, 1 package rows20200627_a85c4933-62ae-ccd9-e053-2a95a90a364b.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75539-00375539-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
LINALOOL, (+/-)-D81QY6I88EIACT
BENZYL BENZOATEN863NB338GIACT
METHYL DIHYDROJASMONATE (SYNTHETIC)3GW44CIE3YIACT
LIMONENE, (+)-GFD7C86Q1WIACT
ETHYL MALTOLL6Q8K29L05IACT
ETHYLENE BRASSYLATE9A87HC7RODIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
.ALPHA.-METHYLBENZYL ACETATEFYS3E9NBA3IACT
.GAMMA.-UNDECALACTONEQB1T0AG2YLIACT

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
a85c4933-62af-ccd9-e053-2a95a90a364ba85c4933-62ae-ccd9-e053-2a95a90a364b2020-06-18Exact identifier
spl id: a85c4933-62af-ccd9-e053-2a95a90a364b
spl set id: a85c4933-62ae-ccd9-e053-2a95a90a364b

Reported adverse events (FAERS/openFDA)#

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