FDA.reportPublic FDA data

Kentex Bathing Cloth

Manufacturer
HAINING LILY CLEANING PRODUCTS CO., LTD
Effective date
2024-03-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:10:14

Label at a glance#

ProductKentex Bathing Cloth
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Wet body thoroughly with product and allow o dry 20-30 seconds. Do no dry or wipe when finished

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE .......... 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

For body-washng to decrease bacteria on the skin when water is not available

Warning

WARNINGS SECTION

  • For external use only.
  • When using this product, do not get in eyes; do not use on open or broken skin, if contact occurs, rinse eyes throughly with water
  • Stop use and ask a doctor, if irritaion and redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

●If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet body thoroughly with product and allow o dry 20-30 seconds. Do no dry or wipe when finished

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, 2-bromo-2-nitro-1, 3-pproanediol, Chitosan Polysorbate 20, Sodium Bezoate, Citric Acid, Aloe Vera

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label imagelabel image

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
77435-30077435-300-01

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
WATER059QF0KO0RIACT
POLYSORBATE 207T1F30V5YHIACT
SODIUM BENZOATEOJ245FE5EUIACT
ACETYLTRIETHYL CITRATE5WBR36T90EIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
f383bb7f-d2b8-4bc5-bad8-e956d38303655901e383-c35b-48cb-bdde-fb934ed58e852024-03-10WarningsExact identifier
spl set id: 5901e383-c35b-48cb-bdde-fb934ed58e85

Reported adverse events (FAERS/openFDA)#

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