FDA.reportPublic FDA data

EARTH EDITION HAND SANITIZER

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
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EARTH EDITION HAND SANITIZEREARTH EDITION HAND SANITIZER

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
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

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
76841-1108-22022-07-29C16284748780-1e4f33bdf-a7ed-d8a0-e053-dadaa90a6e4eEARTH EDITION HAND SANITIZER 110 mL 76841-1108-2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76841-1108-2EARTH EDITION HAND SANITIZER110 mL in 1 BOTTLE, SPRAYLIQUID1101
76841-1108-2EARTH EDITION HAND SANITIZER1 in 1 BOXLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76841-1108EARTH EDITION HAND SANITIZER (ALCOHOL) LIQUID [EARTH EDITION INC.]1Legacy NDC, 2 package rows20200511_a557a2e7-7792-0fe2-e053-2a95a90a37ca.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
76841-110876841-1108-2

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
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
a557aa9e-ad7f-1a54-e053-2995a90af241a557a2e7-7792-0fe2-e053-2a95a90a37ca2020-05-10Exact identifier
spl id: a557aa9e-ad7f-1a54-e053-2995a90af241
spl set id: a557a2e7-7792-0fe2-e053-2a95a90a37ca

Reported adverse events (FAERS/openFDA)#

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