FDA.reportPublic FDA data

HAND SANITIZING WIPES

Manufacturer
Mid-States Distributing, LLC | Tianjin Zejun Int'l Trade Co., Ltd | Cangzhou Juyuan Sanitary Prducts Co., Ltd
Effective date
2021-12-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:45:31

Label at a glance#

ProductHAND SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Dosage and administration

thoroughly wipe skin as desired. allow to dry without wiping. discard wipe after use, do not flush.

Storage and handling

Store in a cool, dry place. Avoid freezing temperatures and excessive heat

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.45% w/w. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Wipes to help reduce bacteria that can potentially cause disease or illness. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on sensitive areas or open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.







Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.







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

OTC - STOP USE SECTION

Stop use and consult doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • thoroughly wipe skin as desired.
  • allow to dry without wiping.
  • discard wipe after use, do not flush.

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool, dry place.
  • Avoid freezing temperatures and excessive heat

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe extract, citric acid, glycerin, propylene glycol, purified water USP.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 Wipes in 1 Canister NDC: 81329-5667-1 Package LabelPackage Label

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

200 Wipes in 1 Canister NDC: 81329-5667-2 Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2377435benzalkonium chloride 0.45 % Medicated PadPSN2
2377435benzalkonium chloride 4.5 MG/ML Medicated PadSCD2
2377435benzalkonium chloride 0.45 % Medicated PadSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81329-5667-12023-01-30C16284748780-1f386c649-c1ce-0266-e053-dadaa90a7c1ab9ca97ee-f7c8-0a45-e053-2a95a90a1c5a
81329-5667-22023-01-30C16284748780-1f386c649-c1ce-0266-e053-dadaa90a7c1ab9ca97ee-f7c8-0a45-e053-2a95a90a1c5a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81329-5667-1HAND SANITIZING WIPES600 g in 1 CANISTERCLOTH6002
81329-5667-2HAND SANITIZING WIPES1000 g in 1 CANISTERCLOTH10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81329-5667HAND SANITIZING WIPES (HAND SANITIZER) CLOTH [MID-STATES DISTRIBUTING, LLC]2Legacy NDC, 2 package rows20211209_b9ca97ee-f7c8-0a45-e053-2a95a90a1c5a.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81329-566781329-5667-1, 81329-5667-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOEV5VD430YW9IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
d29d3621-1cc7-35bc-e053-2a95a90ae70eb9ca97ee-f7c8-0a45-e053-2a95a90a1c5a2021-12-08WarningsExact identifier
spl id: d29d3621-1cc7-35bc-e053-2a95a90ae70e
spl set id: b9ca97ee-f7c8-0a45-e053-2a95a90a1c5a

Reported adverse events (FAERS/openFDA)#

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