WET WIPES

Manufacturer
Ningbo Chenxing Daily Necessities Co., Ltd.
Effective date
2020-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:24:30

Label at a glance#

ProductWET WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Discard wipes in trash receptacle after use. Do not flush. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Wet Wipes

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For 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

When using this product do not use in or near the eyes.

In case of eye contact, rinse eyes thoroughly eyes with water.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Discard wipes in trash receptacle after use. Do not flush.
  • Children under 6 years of age should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75662-004-01 100 wipes

PDPPDP

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
75662-00475662-004-01

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
a95c52bd-29c9-1584-e053-2995a90ad68da8cfc4ef-c011-3e46-e053-2a95a90a11292020-07-01WarningsExact identifier
spl set id: a8cfc4ef-c011-3e46-e053-2a95a90a1129

Reported adverse events (FAERS/openFDA)#

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