Sanitizing Wipes

Manufacturer: Kunming Ansheng Industry & Trade Co., Ltd.
Effective date: 2020-07-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:19:52

Label at a glance#

ProductSanitizing Wipes

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

1, Open sticker, pull out the wipe and close sticker tightly. 2, Dispose of used wipes in trash, DO NOT FLUSH.

Storage and handling

Store between 15-30℃ (59-86F) Avoid freezing and excessive heat about 40℃ (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v;

Chlorohexidine Diacetate 0.1% v/v;

Benzalkonium 0.1% v/v;

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacterial on the skin.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

on infants less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be 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 contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

1, Open sticker, pull out the wipe and close sticker tightly.

2, Dispose of used wipes in trash, DO NOT FLUSH.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30℃ (59-86F)
Avoid freezing and excessive heat about 40℃ (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Chlorohexidine Diacetate, Benzalkonium Chloride, Nano Silver Ion (Ag+)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80 wipes in 1 bag. NDC: 78183-002-01;

80pcs

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78183-002-01	2022-01-28	C162847	48780-1	d6a99b39-f6d7-a426-e053-dadaa90af4c2	Defendmax Sanitizing Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78183-002-01	Sanitizing Wipes	80 U in 1 BAG	CLOTH	80		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78183-002	SANITIZING WIPES (DEFENDMAX SANITIZING WIPES) CLOTH [KUNMING ANSHENG INDUSTRY & TRADE CO., LTD.]	1	Legacy NDC, 1 package rows	20200702_a96ef5a2-622c-91dd-e053-2995a90a05e1.zip

Products#

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

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

Sanitizing Wipes
Defendmax Sanitizing Wipes
SILVER ACETATE
CHLORHEXIDINE ACETATE
BENZALKONIUM CHLORIDE
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78183-002	78183-002-01

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
SILVER ACETATE	19PPS85F9H	IACT
CHLORHEXIDINE ACETATE	5908ZUF22Y	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
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
a96ef5a2-622b-91dd-e053-2995a90a05e1			a96ef5a2-622c-91dd-e053-2995a90a05e1	2020-07-02	Warnings	Exact identifier spl id: a96ef5a2-622b-91dd-e053-2995a90a05e1 spl set id: a96ef5a2-622c-91dd-e053-2995a90a05e1

Reported adverse events (FAERS/openFDA)#

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