FDA.reportPublic FDA data

Antiseptic Hand Sanitizer Wipes

Manufacturer
Eco Wipes Vietnam Corporation
Effective date
2020-07-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:59

Label at a glance#

ProductAntiseptic Hand Sanitizer Wipes
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.
Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other information

SPL UNCLASSIFIED SECTION

  • Store in cool and dry place, away from direct sunlight
  • Close the lid to maintain quality and cleanliness
  • Do not use as a diaper wipe
  • Do not flush down the toilet

Inactive ingredients

INACTIVE INGREDIENT SECTION

2-Bromo-2-Nitropropane-1,3-Diol, Aloe Vera, Disodium Cocoamphodiacetate, Glycerin, Lemon extract, PEG 40 Hydrogenated Castor oil, Phenoxyethanol, Propylene Glycol, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78898-000-202023-01-30C16284748780-1f386c649-c728-0266-e053-dadaa90a7c1aAntiseptic Hand Sanitizer Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78898-000-20Antiseptic Hand Sanitizer Wipes20 in 1 PACKAGEPATCH201
78898-000-20Antiseptic Hand Sanitizer Wipes6 mL in 1 PATCHPATCH61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78898-000ANTISEPTIC HAND SANITIZER WIPES (ALCOHOL) PATCH [ECO WIPES VIETNAM CORPORATION]1Legacy NDC, 2 package rows20200703_a97b7dfa-d048-71f0-e053-2995a90a5ceb.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78898-00078898-000-20

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
BRONOPOL6PU1E16C9WIACT
ALOE VERA LEAFZY81Z83H0XIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
GLYCERINPDC6A3C0OXIACT
LEMON24RS0A988OIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
a97b833c-357e-ddc4-e053-2a95a90a5344a97b7dfa-d048-71f0-e053-2995a90a5ceb2020-07-02WarningsExact identifier
spl id: a97b833c-357e-ddc4-e053-2a95a90a5344
spl set id: a97b7dfa-d048-71f0-e053-2995a90a5ceb

Reported adverse events (FAERS/openFDA)#

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