ELEMENTS ETHANOL 75% HAND SANITIZER WIPES

Manufacturer
URBANBCL CO LTD
Effective date
2020-07-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:04

Label at a glance#

ProductELEMENTS ETHANOL 75% HAND SANITIZER WIPES
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ethyl alcohol

OTC - PURPOSE SECTION

Hand sanitizing wipes to help reduce bacteria that potentially can cause disease

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

Water, Dipropylene Glycol, Fragrance, Aloe Extract

INDICATIONS & USAGE SECTION

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

■ Do not flush

■ Children under 2 years ask a doctor before use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
74200-0032-12021-07-23C16284748780-1c7ccaba7-14dc-fd44-e053-dadaa90aa01bDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74200-0032-1ELEMENTS ETHANOL 75% HAND SANITIZER WIPES80 mL in 1 PACKAGELIQUID801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74200-0032ELEMENTS ETHANOL 75% HAND SANITIZER WIPES (ALCOHOL) LIQUID [URBANBCL CO LTD]1Legacy NDC, 1 package rows20200721_aae9359a-b1e4-c827-e053-2a95a90a73b4.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
74200-003274200-0032-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
aae9230d-c012-310f-e053-2a95a90ad6b5aae9359a-b1e4-c827-e053-2a95a90a73b42020-07-20WarningsExact identifier
spl id: aae9230d-c012-310f-e053-2a95a90ad6b5
spl set id: aae9359a-b1e4-c827-e053-2a95a90a73b4

Reported adverse events (FAERS/openFDA)#

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