ALCOHOL WIPES

Manufacturer: Zhejiang Huanghua Biological Technology Co., Ltd
Effective date: 2020-10-29
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:32:38

Label at a glance#

ProductALCOHOL WIPES

Active ingredientALCOHOL, BENZALKONIUM CHLORIDE, METHYLISOTHIAZOLINONE, PROPYLENE GLYCOL, PHENOXYETHANOL

Label structure9 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

store between 15-30°C(59-86°F),avoid freezing and excessive heat above 40°C(104°F)

INACTIVE INGREDIENT SECTION

pure water

INDICATIONS & USAGE SECTION

1.Open cover and remove seal.
2.Pull out wipe corner from center of the roll.
3.Thread through hole in the cover.
4.Close lid after use to retain moisture.

OTC - ACTIVE INGREDIENT SECTION

alcohol

Benzalkamine

2-methyl-4-isothiazoline-3-one

propylene glyco

2-phenoxyethanol

OTC - DO NOT USE SECTION

Stop use and ask a doctor if irritation or rash occurs.These maybe signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41546-009-01	ALCOHOL WIPES	80 in 1 PAIL	CLOTH	80		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41546-009	ALCOHOL WIPES CLOTH [ZHEJIANG HUANGHUA BIOLOGICAL TECHNOLOGY CO., LTD]	2	Legacy NDC, 1 package rows	20201030_aeed7e1d-7ad8-7eff-e053-2995a90a1ca8.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

ALCOHOL WIPES
ALCOHOL
BENZALKONIUM CHLORIDE
BENZALKONIUM
METHYLISOTHIAZOLINONE
PROPYLENE GLYCOL
PHENOXYETHANOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41546-009	41546-009-01

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
METHYLISOTHIAZOLINONE	229D0E1QFA	ACTIB
PROPYLENE GLYCOL	6DC9Q167V3	ACTIB
PHENOXYETHANOL	HIE492ZZ3T	ACTIB
WATER	059QF0KO0R	IACT

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
b2db2f61-2ecb-a5bf-e053-2a95a90a00e8			aeed7e1d-7ad8-7eff-e053-2995a90a1ca8	2020-10-29	Warnings	Exact identifier spl id: b2db2f61-2ecb-a5bf-e053-2a95a90a00e8 spl set id: aeed7e1d-7ad8-7eff-e053-2995a90a1ca8

Reported adverse events (FAERS/openFDA)#

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