FDA.reportPublic FDA data

Triple X Sanitizing Wipes

Manufacturer
Zhangzhou Zhongnan Nursing Products Co., Ltd.
Effective date
2020-08-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:27

Label at a glance#

ProductTriple X Sanitizing Wipes
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

To help reduce bacteria that potentially can cause disease

Dosage and administration

Open the pouch and wipe the desired area with the tissue.

Storage and handling

Store in a cool dry place.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethanol Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria that potentially can cause disease

Directions

DOSAGE & ADMINISTRATION SECTION

Open the pouch and wipe the desired area with the tissue.

Warnings

WARNINGS SECTION

This is a single use product, once opened, please use immediately to avoid loss of moisture.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Supervise children under 6 years of ages when using this product to avoid swallowing.

Storage

STORAGE AND HANDLING SECTION

Store in a cool dry place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Benzethonium Chloride, Aloe Barbadensis Extract.

Package Label/Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 79650-003-07 (200 ml)

Triple X Sanitizing WipesTriple X Sanitizing Wipes

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79650-003-072021-07-23C16284748780-1c7ccaba7-1f7d-fd44-e053-dadaa90aa01bac0dc8fb-7b99-626c-e053-2a95a90a13b4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79650-003-07Triple X Sanitizing Wipes200 mL in 1 BAGLIQUID2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79650-003TRIPLE X SANITIZING WIPES (SANITIZING WIPES) LIQUID [ZHANGZHOU ZHONGNAN NURSING PRODUCTS CO., LTD.]1Legacy NDC, 1 package rows20200812_ac0dc8fb-7b99-626c-e053-2a95a90a13b4.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79650-00379650-003-07

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
NameUNIIKind
BENZETHONIUM CHLORIDEPH41D05744IACT
ALOEV5VD430YW9IACT
ALCOHOL3K9958V90MACTIB
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
ac0dc8fb-7b9a-626c-e053-2a95a90a13b4ac0dc8fb-7b99-626c-e053-2a95a90a13b42020-08-11WarningsExact identifier
spl id: ac0dc8fb-7b9a-626c-e053-2a95a90a13b4
spl set id: ac0dc8fb-7b99-626c-e053-2a95a90a13b4

Reported adverse events (FAERS/openFDA)#

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