FDA.reportPublic FDA data

ZERO-PERCENT Portable Sanitizer

Manufacturer
Ester Co., Ltd.
Effective date
2020-10-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:07

Label at a glance#

ProductZERO-PERCENT Portable Sanitizer
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZERO-PERCENT Portable SanitizerZERO-PERCENT Portable 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
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74004-041-022022-01-28C16284748780-1d6a99b39-e390-a426-e053-dadaa90af4c2[1] ZERO-PERCENT Portable Sanitizer (Fragrance) 74004-041-02 Blister package, 4 colors

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74004-041-02ZERO-PERCENT Portable Sanitizer40 mL in 1 BOTTLE, SPRAYSPRAY401
74004-041-02ZERO-PERCENT Portable Sanitizer1 in 1 BLISTER PACKSPRAY11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74004-041ZERO-PERCENT PORTABLE SANITIZER (ALCOHOL) SPRAY [ESTER CO., LTD.]1Legacy NDC, 2 package rows20201007_b10a1752-a1ef-599f-e053-2995a90a5469.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
74004-04174004-041-02

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
ALOE ARBORESCENS LEAF09TD8L5SQVIACT

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
b10a1752-a1f0-599f-e053-2995a90a5469b10a1752-a1ef-599f-e053-2995a90a54692020-10-06Exact identifier
spl id: b10a1752-a1f0-599f-e053-2995a90a5469
spl set id: b10a1752-a1ef-599f-e053-2995a90a5469

Reported adverse events (FAERS/openFDA)#

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