FDA.reportPublic FDA data

EARTH EDITION HAND SANITIZER Gel

Manufacturer
Earth Edition Inc. | Skin n Skin Co., Ltd.
Effective date
2020-05-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:41

Label at a glance#

ProductEARTH EDITION HAND SANITIZER Gel
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EARTH EDITION HAND SANITIZER GelEARTH EDITION HAND SANITIZER Gel

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76841-4806-12022-07-29C16284748780-1e4f33bdf-ac3b-d8a0-e053-dadaa90a6e4eEARTH EDITION HAND SANITIZER Gel 480 mL 76841-4806-1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76841-4806-1EARTH EDITION HAND SANITIZER Gel480 mL in 1 BOTTLE, PUMPGEL4801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76841-4806EARTH EDITION HAND SANITIZER GEL (ETHANOL) GEL [EARTH EDITION INC.]1Legacy NDC, 1 package rows20200511_a5583d17-6022-1902-e053-2a95a90a9f01.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76841-480676841-4806-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
GLYCERINPDC6A3C0OXIACT
ALLANTOIN344S277G0ZIACT
ORANGE OILAKN3KSD11BIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
PANTHENOLWV9CM0O67ZIACT
ALCOHOL3K9958V90MACTIB
LIMONENE, (+)-GFD7C86Q1WIACT

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
a5583d17-6023-1902-e053-2a95a90a9f01a5583d17-6022-1902-e053-2a95a90a9f012020-05-10Exact identifier
spl id: a5583d17-6023-1902-e053-2a95a90a9f01
spl set id: a5583d17-6022-1902-e053-2a95a90a9f01

Reported adverse events (FAERS/openFDA)#

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