FDA.reportPublic FDA data

Hand Sanitizer Gel

Manufacturer
Cerberus Craft Distillery LLC
Effective date
2020-11-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:34:04

Label at a glance#

ProductHand Sanitizer Gel
Active ingredientALCOHOL
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80%Ethyl Alcohol 80%

INDICATIONS & USAGE SECTION

1 gallon1 gallon

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16oz Hand Sanitizer Gel16oz Hand Sanitizer Gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN3
1041498ethanol 0.8 ML/ML Topical GelSCD3
1041498ethanol 80 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74592-003-022022-01-28C16284748780-1d6a99b39-b393-a426-e053-dadaa90af4c2Hand Sanitizer gel 80%
74592-003-042022-01-28C16284748780-1d6a99b39-b393-a426-e053-dadaa90af4c2Hand Sanitizer gel 80%
74592-003-162022-01-28C16284748780-1d6a99b39-b393-a426-e053-dadaa90af4c2Hand Sanitizer gel 80%
74592-003-342022-01-28C16284748780-1d6a99b39-b393-a426-e053-dadaa90af4c2Hand Sanitizer gel 80%
74592-003-692022-01-28C16284748780-1d6a99b39-b393-a426-e053-dadaa90af4c2Hand Sanitizer gel 80%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74592-003-02Hand Sanitizer Gel2 g in 1 BOTTLE, DISPENSINGGEL23
74592-003-04Hand Sanitizer Gel4 g in 1 BOTTLE, DISPENSINGGEL43
74592-003-16Hand Sanitizer Gel16 g in 1 BOTTLE, DISPENSINGGEL163
74592-003-34Hand Sanitizer Gel3.4 g in 1 BOTTLE, DISPENSINGGEL3.43
74592-003-69Hand Sanitizer Gel6.9 g in 1 BOTTLE, DISPENSINGGEL6.93

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74592-003HAND SANITIZER GEL (ETHYL ALCOHOL) GEL [CERBERUS CRAFT DISTILLERY LLC]3Legacy NDC, 5 package rows20201122_a887dee3-f706-d78f-e053-2a95a90ae748.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74592-00374592-003-16, 74592-003-34, 74592-003-02, 74592-003-04, 74592-003-69

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
AMINOMETHYL PROPANEDIOLCZ7BU4QZJZIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT

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
b4a61c44-87c1-29ca-e053-2995a90a3b31a887dee3-f706-d78f-e053-2a95a90ae7482020-11-21Exact identifier
spl id: b4a61c44-87c1-29ca-e053-2995a90a3b31
spl set id: a887dee3-f706-d78f-e053-2a95a90ae748

Reported adverse events (FAERS/openFDA)#

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