FDA.reportPublic FDA data

Alcohol disinfectant wipes

Manufacturer
Zhejiang Huanghua Biological Technology Co., Ltd
Effective date
2020-12-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:44

Label at a glance#

ProductAlcohol disinfectant wipes
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE, METHYLISOTHIAZOLINONE, PROPYLENE GLYCOL, PHENOXYETHANOL
Label structure10 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

open the package lid and wipe skin until dry.

OTC - ACTIVE INGREDIENT SECTION

alcohol

Benzalkamine

2-methyl-4-isothiazoline-3-one

propylene glyco

2-phenoxyethanol

OTC - DO NOT USE SECTION

For children less than 2 months of age.

On open skin wounds.

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.

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

OTC - STOP USE SECTION

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

WARNINGS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41546-016-012022-01-28C16284748780-1d6a99b39-b424-a426-e053-dadaa90af4c2b5dbc6ab-acfc-87a0-e053-2a95a90a69c3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41546-016-01Alcohol disinfectant wipes50 in 1 BAGCLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41546-016ALCOHOL DISINFECTANT WIPES CLOTH [ZHEJIANG HUANGHUA BIOLOGICAL TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20201208_b5dbc6ab-acfc-87a0-e053-2a95a90a69c3.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41546-01641546-016-01

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
ALCOHOL3K9958V90MACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
METHYLISOTHIAZOLINONE229D0E1QFAACTIB
PROPYLENE GLYCOL6DC9Q167V3ACTIB
PHENOXYETHANOLHIE492ZZ3TACTIB
WATER059QF0KO0RIACT

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
b5dbc6ab-acfd-87a0-e053-2a95a90a69c3b5dbc6ab-acfc-87a0-e053-2a95a90a69c32020-12-07WarningsExact identifier
spl id: b5dbc6ab-acfd-87a0-e053-2a95a90a69c3
spl set id: b5dbc6ab-acfc-87a0-e053-2a95a90a69c3

Reported adverse events (FAERS/openFDA)#

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