WET WIPES

Manufacturer
Ningbo Chenxing Daily Necessities Co., Ltd.
Effective date
2020-05-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:09:17

Label at a glance#

ProductWET WIPES
Active ingredientDIDECYLDIMONIUM CHLORIDE, BENZALKONIUM CHLORIDE
Label structure13 sections

Dosage and administration

Surface should be sealed wood, granite, glass and stainless steel. Please test surface prior to usage. Lift seal, pull wipe. Wipe appropriate surface. Let surface air dry. Dispose of wipe in trash. Do not flush wipe.

Storage and handling

Store at a shady, cool and dry place It may discolor certain fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Didecyldimonium Chloride 0.15%. Purpose: Antiseptic

Benzalkonium Chloride 0.1%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Wet Wipes

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on skin

Warnings

WARNINGS SECTION

External use only.

Do not use

OTC - DO NOT USE SECTION

  • if you are allergic to any of the ingredients.
  • on children less than 2 years of age unless directed by a doctor.
  • as a diaper wipe or for personal cleaning

OTC - WHEN USING SECTION

Avoid direct contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if signs of irritation or rash appear.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Surface should be sealed wood, granite, glass and stainless steel. Please test surface prior to usage. Lift seal, pull wipe. Wipe appropriate surface. Let surface air dry. Dispose of wipe in trash. Do not flush wipe.

Other information

STORAGE AND HANDLING SECTION

  • Store at a shady, cool and dry place
  • It may discolor certain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Phenoxyethanol, Ethylhexyl Glycerin, Propylene Glycol, Glycerin

RECENT MAJOR CHANGES SECTION

Indications and Usage

Dosage and Administration

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75662-001-01 80 wipes

PDPPDP

75662-001-02 10 wipes

PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75662-001-012022-01-28C16284748780-1d6a99b39-d848-a426-e053-dadaa90af4c2WET WIPES
75662-001-022022-01-28C16284748780-1d6a99b39-d848-a426-e053-dadaa90af4c2WET WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75662-001-01WET WIPES80 in 1 PACKAGECLOTH803
75662-001-02WET WIPES10 in 1 PACKAGECLOTH103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75662-001WET WIPES CLOTH [NINGBO CHENXING DAILY NECESSITIES CO., LTD.]3Legacy NDC, 2 package rows20200502_a3b39507-8749-791c-e053-2a95a90aea22.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
75662-00175662-001-01, 75662-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a4a39dd9-1be2-6810-e053-2a95a90a4da2a3b39507-8749-791c-e053-2a95a90aea222020-05-02WarningsExact identifier
spl id: a4a39dd9-1be2-6810-e053-2a95a90a4da2
spl set id: a3b39507-8749-791c-e053-2a95a90aea22

Reported adverse events (FAERS/openFDA)#

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