75% Alcohol Wipes

Manufacturer: Hangzhou Eternal Love Personal Care Co., Ltd
Effective date: 2025-08-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:12:08

Label at a glance#

Product75% Alcohol Wipes

Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Purpose: Antiseptic

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethyl alcohol 75%; Benzalkonium Chloride 0.05%

INDICATIONS & USAGE SECTION

Use: For skin only. Do not ingest.

WARNINGS SECTION

Warnings:

Flammability: Flammable. Keep from heat/sparks/flames.

Eye Contact: Avoid contact. Flush with water if contact.

Skin Irritation: Stop use if irritation/redness. Consult doctor.

Open Wounds: Do not use on open wounds unless doctor directs.

Swallowing: If swallowed, seek medical help/poison control.

Storage: Store cool/ventilated. Away from heat, kids/animals.

Repeated Use: Repeated use may dry skin.

DOSAGE & ADMINISTRATION SECTION

Directions of Use:

Open the lid and slowly peel back label.2. Pull out wipes as needed.3. Reseal label to retain moisture.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of Children: Supervise kids <6.

INACTIVE INGREDIENT SECTION

Inactive ingredients: RO pure water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75% Alcohol WipesLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2722591	benzalkonium chloride 0.05 % / ethanol 75 % Medicated Pad	PSN	1
2722591	benzalkonium chloride 0.5 MG/ML / ethanol 0.75 ML/ML Medicated Pad	SCD	1
2722591	benzalkonium chloride 0.05 % / ethanol 75 % Medicated Pad	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
87065-101-01	75% Alcohol Wipes	340 g in 1 BAG	LIQUID	340		1
87065-101-02	75% Alcohol Wipes	40 in 1 BOX	LIQUID	40		1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

75% Alcohol Wipes
Alcohol
BENZALKONIUM CHLORIDE
BENZALKONIUM
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
87065-101	87065-101-01, 87065-101-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	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
3d7d6e73-2a51-cac9-e063-6294a90a7891			3d7d6e73-2a50-cac9-e063-6294a90a7891	2025-08-29	Warnings	Exact identifier spl id: 3d7d6e73-2a51-cac9-e063-6294a90a7891 spl set id: 3d7d6e73-2a50-cac9-e063-6294a90a7891

Reported adverse events (FAERS/openFDA)#

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