The Nordic Shield Sanitizer Wipes

Manufacturer
The Nordic Shield Aps
Effective date
2020-09-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:38

Label at a glance#

ProductThe Nordic Shield Sanitizer Wipes
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For sanitizing to help reduce bacteria on the skin.

Dosage and administration

• Open lid, gently pull back resealable label, remove and use wipe as required. • Reseal back after use to avoid evaporation of alcohol.

Storage and handling

This product is insoluble in water. Dispose of used wipe in trash, do not flush into toilet. This product may discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For sanitizing to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in or near the eyes.

• on open skin wounds or burns

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Open lid, gently pull back resealable label, remove and use wipe as required.

• Reseal back after use to avoid evaporation of alcohol.

Other information

STORAGE AND HANDLING SECTION

This product is insoluble in water. Dispose of used wipe in trash, do not flush into toilet. This product may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua)

SPL UNCLASSIFIED SECTION

Disinfecting Wet Wipes 75% Alcohol

MANUFACTURED BY HENAN YEESSAIN HEALTH TECHNOLOGY CO. LTD.

www.yeesain.com

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

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
79232-900-502022-01-28C16284748780-1d6a99b39-b025-a426-e053-dadaa90af4c2Deyo SANITIZING WET WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79232-900-50The Nordic Shield Sanitizer Wipes6.2 mL in 1 PACKAGECLOTH6.21
79232-900-50The Nordic Shield Sanitizer Wipes50 in 1 PACKETCLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79232-900THE NORDIC SHIELD SANITIZER WIPES (ALCOHOL) CLOTH [THE NORDIC SHIELD APS]1Legacy NDC, 2 package rows20201001_631c894a-84ca-4b7b-bf54-67cc9aea3e1f.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79232-90079232-900-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
8f2d6b81-007f-46cd-b235-6690f47d4b9c631c894a-84ca-4b7b-bf54-67cc9aea3e1f2020-09-09WarningsExact identifier
spl id: 8f2d6b81-007f-46cd-b235-6690f47d4b9c
spl set id: 631c894a-84ca-4b7b-bf54-67cc9aea3e1f

Reported adverse events (FAERS/openFDA)#

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