Wet Wipes

Manufacturer
Hangzhou ChunChi Touring Commodity CO., LTD.
Effective date
2022-10-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:51:38

Label at a glance#

ProductWet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Do not expose to direct sunlight, preferably place them in a coolplace. Do not use on furniture. Do not flush down toilets,dispose in trash recepticals. Remove lid and open the seal. Pull up the corner of the center sheet, twist it and thread nrougnnichadrlose lid flap to retain moisture.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

PURPOSE

OTC - PURPOSE SECTION

Antibacterial

USE

INDICATIONS & USAGE SECTION

decreases bacteria on skin

Warning

WARNINGS SECTION

For external use only
Do not use:Over large areas of the body ifyou are allergicto any ofthe ingredients.
When using this product do not get into eyes.If contactoccurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash develops andcontinues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
For children under 2 years ask a doctor before use.For childrenuse under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

Do not expose to direct sunlight, preferably place them in a coolplace. Do not use on furniture. Do not flush down toilets,dispose in trash recepticals.
Remove lid and open the seal. Pull up the corner of the center sheet, twist it and thread nrougnnichadrlose lid flap to retain moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol,Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate,Fragrance,Benzyl
Alcohol,Methylchloroisothiazolinone,Methylisothiazolinone, Tetrasodium EDTA, PEG-40 Hydrogenated Castor Oil, Centrimonium Chloride, Citric Acid,Aloe Vera Extract, Alphatocopherol Acetate (Vitamin E)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81361-00281361-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
eafd2305-1396-1f32-e053-2995a90aa0c8eafd2305-1395-1f32-e053-2995a90aa0c82022-10-14WarningsExact identifier
spl id: eafd2305-1396-1f32-e053-2995a90aa0c8
spl set id: eafd2305-1395-1f32-e053-2995a90aa0c8

Reported adverse events (FAERS/openFDA)#

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