Caseys

Manufacturer: Zhejiang Bright Care Co., Ltd.
Effective date: 2025-08-30
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:12:10

Label at a glance#

ProductCaseys

Active ingredientBENZALKONIUM CHLORIDE

Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

BENZALKONIUM CHLORIDE 0.13%

OTC - PURPOSE SECTION

Purpose

Antibacterial

INDICATIONS & USAGE SECTION

Uses

To decrease bacteria on the skin
Recommended for repeated use

WARNINGS SECTION

Warnings

For external use only.

OTC - WHEN USING SECTION

When using this product, keep away from eyes. In case of eye contact, rinse eyes with water

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or redness develops or lasts for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions:

rub wipe thoroughly over all surfaces of both hands
allow to dry without wiping
superwise children under 6 years old
not recommended for infants
dispose of wipe in trash, do not flush

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Fragrance, C12-15 Alcohols, Chloroxylenol, Aloe Barbadensis Leaf Juice

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1038558	Benzalkonium (Topical)	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD Active
1049254	Benzalkonium (Topical)	benzalkonium chloride 1.3 MG/ML Topical Solution	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1049254	benzalkonium chloride 0.13 % Topical Solution	PSN	1
1049254	benzalkonium chloride 1.3 MG/ML Topical Solution	SCD	1
1049254	benzalkonium chloride 0.13 % Topical Solution	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85844-001-01	Caseys	3.6 g in 1 PATCH	SOLUTION	3.6		1
85844-001-01	Caseys	15 in 1 POUCH	SOLUTION	15		1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Caseys
BENZALKONIUM CHLORIDE
WATER
CHLOROXYLENOL
C12-15 ALCOHOLS
ALOE BARBADENSIS LEAF JUICE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85844-001	85844-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CHLOROXYLENOL	0F32U78V2Q	IACT
C12-15 ALCOHOLS	2C8M6XLB5C	IACT
ALOE BARBADENSIS LEAF JUICE	RUE8E6T4NB	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Caseys	BENZALKONIUM CHLORIDE	Zhejiang Bright Care Co., Ltd.	a29d6c19-01aa-45b0-92cd-3f1148bad4f8	2025-08-30	Warnings	Exact identifier ndc (package): 85844-001-01 ndc (product): 85844-001 ndc11 (package): 85844000101 spl id: 3d95e6a8-8801-17b9-e063-6394a90ab728 spl set id: a29d6c19-01aa-45b0-92cd-3f1148bad4f8

Reported adverse events (FAERS/openFDA)#

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