FDA.reportPublic FDA data

Disinfecting wipes

Manufacturer
Nanofixit Ventures Inc. | Xiamen Ekem Tech.co.,ltd.
Effective date
2020-07-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:24

Label at a glance#

ProductDisinfecting wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Wipe surface thoroughly with product and let dry. Discard wipe in trash properly. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.2% w/w. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on 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 ask a 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 except with adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wipe surface thoroughly with product and let dry. Discard wipe in trash properly.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citric Acid, Didecyl Dimethyl Ammonium Chloride, Glycerin, Vitamin E, Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80 WIPES in 1 PIAL NDC: 92763-004-01 Package LabelPackage Label

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

800 WIPES in 1 BAG NDC: 92763-004-02 Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2360919benzalkonium Cl 0.2 % Medicated PadPSN1
2360919benzalkonium chloride 2 MG/ML Medicated PadSCD1
2360919benzalkonium chloride 0.2 % Medicated WipeSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
92763-004-012022-01-28C16284748780-1d6a99b39-4476-a426-e053-dadaa90af4c2aba5f862-1462-52ac-e053-2a95a90af2de
92763-004-022022-01-28C16284748780-1d6a99b39-4476-a426-e053-dadaa90af4c2aba5f862-1462-52ac-e053-2a95a90af2de

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
92763-004-01Disinfecting wipes432 g in 1 PAILCLOTH4321
92763-004-02Disinfecting wipes4320 g in 1 BAGCLOTH43201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
92763-004DISINFECTING WIPES (HAND SANITIZER) CLOTH [NANOFIXIT VENTURES INC.]1Legacy NDC, 2 package rows20200801_aba5f862-1462-52ac-e053-2a95a90af2de.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
92763-00492763-004-01, 92763-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
TOCOPHEROLR0ZB2556P8IACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
GLYCERINPDC6A3C0OXIACT
ALOEV5VD430YW9IACT
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
aba5f862-144f-52ac-e053-2a95a90af2deaba5f862-1462-52ac-e053-2a95a90af2de2020-07-30WarningsExact identifier
spl id: aba5f862-144f-52ac-e053-2a95a90af2de
spl set id: aba5f862-1462-52ac-e053-2a95a90af2de

Reported adverse events (FAERS/openFDA)#

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