Antiseptic Hand Wipe

Manufacturer: Metro Medical Equipment Mfg. Inc | Xiamen Yiukin Paper Products Co.,ltd
Effective date: 2020-08-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:14

Label at a glance#

ProductAntiseptic Hand Wipe

Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL

Label structure11 sections

Dosage and administration

Remove and unfold wipe from package Wipe hands and nails thoroughly Allow skin to dry without wiping Discard properly Single Use Only

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Remove and unfold wipe from package

Wipe hands and nails thoroughly

Allow sking to dry without wiping

Discard Properly

Single Use Only

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 15%

Benzalkonium Chloride .1%

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PURPOSE SECTION

Antiseptic

INTENDED USE OF THE DEVICE

Hand sanitizer to help reduce bacteria on the skin.

WARNINGS SECTION

Flammable

Keep away from fire or flame

For external use only

When using this product aboid use near eyes

If contact occurs, rinse thoroughly with water

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children

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

Directions

INSTRUCTIONS FOR USE SECTION

Remove and unfold wipe from package

Wipe hands and nails thoroughly

Allow skin to dry without wiping

Discard properly

Single Use Only

Other

OTHER SAFETY INFORMATION

Store at room temperature

INACTIVE INGREDIENT SECTION

Propylene glycol

Phenoxyethanol

Cetylpyridinium Chloride

Water

spunlace non-woven fabric

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelBack LabelBack Label Continued

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2396017	benzalkonium chloride 0.1 % / ethanol 15 % Medicated Pad	PSN	1
2396017	benzalkonium chloride 1 MG/ML / ethanol 0.15 ML/ML Medicated Pad	SCD	1
2396017	benzalkonium chloride 0.1 % / ethanol 15 % Medicated Pad	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
90024-001-01	2022-01-28	C162847	48780-1	d6a99b39-7ab6-a426-e053-dadaa90af4c2	addeb1f3-161b-4a4d-e053-2995a90aca9e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
90024-001-01	Antiseptic Hand Wipe	6.5 g in 1 PACKAGE	CLOTH	6.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
90024-001	ANTISEPTIC HAND WIPE (ALCOHOL, BENZALKONIUM CHLORIDE) CLOTH [METRO MEDICAL EQUIPMENT MFG. INC]	1	Legacy NDC, 1 package rows	20200829_addeb1f3-161b-4a4d-e053-2995a90aca9e.zip

Products#

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

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

Antiseptic Hand Wipe
Alcohol, Benzalkonium Chloride
BENZALKONIUM CHLORIDE
BENZALKONIUM
PHENOXYETHANOL
CETYLPYRIDINIUM CHLORIDE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
90024-001	90024-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PHENOXYETHANOL	HIE492ZZ3T	IACT
CETYLPYRIDINIUM CHLORIDE	D9OM4SK49P	IACT
ALCOHOL	3K9958V90M	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
addeb1f3-161c-4a4d-e053-2995a90aca9e			addeb1f3-161b-4a4d-e053-2995a90aca9e	2020-08-27	Warnings	Exact identifier spl id: addeb1f3-161c-4a4d-e053-2995a90aca9e spl set id: addeb1f3-161b-4a4d-e053-2995a90aca9e

Reported adverse events (FAERS/openFDA)#

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