FELIX Hand Sanitizer Gel

Manufacturer
Ester Co., Ltd.
Effective date
2020-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:05

Label at a glance#

ProductFELIX Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FELIX HAND SANITIZER GEL 500 mlFELIX HAND SANITIZER GEL 500 ml

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809563705795GTIN-13: 8809563705795
EAN-13: 8809563705795
GTIN storage (14 digits): 08809563705795
FELIX 500 mL.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74004-702-012022-01-28C16284748780-1d6a99b39-f294-a426-e053-dadaa90af4c2[Ester Co., Ltd.-FELIX HAND SANITIZER GEL] 500 ml : BOTTLE+PUMP : 74004-702-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74004-702-01FELIX Hand Sanitizer Gel500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74004-702FELIX HAND SANITIZER GEL (ALCOHOL) GEL [ESTER CO., LTD.]1Legacy NDC, 1 package rows20200521_a6250431-e7ea-3df1-e053-2a95a90a1659.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74004-70274004-702-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
a62507d9-048c-139f-e053-2995a90a2bc9a6250431-e7ea-3df1-e053-2a95a90a16592020-05-21Exact identifier
spl id: a62507d9-048c-139f-e053-2995a90a2bc9
spl set id: a6250431-e7ea-3df1-e053-2a95a90a1659

Reported adverse events (FAERS/openFDA)#

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