Sanitizing Alcohol Free Wipes

Manufacturer
Shedrain Corporation | Zhangzhou Zhongnan Nursing Products Co., Ltd
Effective date
2020-10-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:18

Label at a glance#

ProductSanitizing Alcohol Free Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient for this sanitizing alcohol-free wipes is Benzalkonium chloride

. Active ingredientActive ingredient

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer to help decrease bacteria on the skin. PurposePurpose

Use

INDICATIONS & USAGE SECTION

For dispensing: Peel back front label at tab. Remove towelette wipes as needed. Reseal pouch by pressing label firmly back into place.

For use: Apply thoroughly to hands as desired. Allow to dry without wiping. Discard wipe in trash after use. Do not flush.

IndicationIndication

Warnings

WARNINGS SECTION

For external use only.

warningwarning

Do not use

OTC - DO NOT USE SECTION

Do not use in or near the eyes. If contact occurs, flush thoroughly with water.

Do not useDo not use

OTC - STOP USE SECTION

Stop use and contact doctor if redness and irritation develops and persists.

Stop useStop use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of childrenKeep out of children

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Polyaminopropyl Biguanide, Xylitol Extract, Aloe Barbadensis Leaf Extract.

Inactive ingredientInactive ingredient

Dosage

DOSAGE & ADMINISTRATION SECTION

FOR DISPENSING: Peel back front label at tab. Remove towelette wipes as needed.

FOR USE: Apply thoroughly to hands asdesired. Allow to dry without wiping.

Dosage and administrationDosage and administration

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20-pack. NDC: 80380-100-01

. Package labelPackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80380-100-012021-07-23C16284748780-1c7ccaba7-204f-fd44-e053-dadaa90aa01bb1c1c819-e35a-6c60-e053-2a95a90aa104

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80380-100-01Sanitizing Alcohol Free Wipes20 mg in 1 PACKETCLOTH201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80380-100SANITIZING ALCOHOL FREE WIPES CLOTH [SHEDRAIN CORPORATION]1Legacy NDC, 1 package rows20201023_b1c1c819-e35a-6c60-e053-2a95a90aa104.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80380-10080380-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b1c1c819-e34c-6c60-e053-2a95a90aa104b1c1c819-e35a-6c60-e053-2a95a90aa1042020-10-23WarningsExact identifier
spl id: b1c1c819-e34c-6c60-e053-2a95a90aa104
spl set id: b1c1c819-e35a-6c60-e053-2a95a90aa104

Reported adverse events (FAERS/openFDA)#

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