FDA.reportPublic FDA data

ZAPRO HAND SANITIZER

Manufacturer
GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.
Effective date
2020-12-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:54

Label at a glance#

ProductZAPRO HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Press pump twice to dever two s quits of product on to the pam of your hand Rub hands together and allow to dry without wiping

Storage and handling

May discolor fabrics or surfaces Store below 110°F(43°C)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 94%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use
for hand washing to decrease bacteria on he skin， only when water is not ava able

Warnings

WARNINGS SECTION

Flammable—Keep away from fire and flames
For external use only

Do not use

OTC - DO NOT USE SECTION

Do not get into eyes
lf contact occurs， rinse thoroughly with water

When using this product

OTC - WHEN USING SECTION

When using this product
Do not get into eyes
lf contact occurs， rinse thoroughly with water

Stop use and ask a doctor if
Irritation and redness develop

Keep out of reach of children.If swallowed， get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if
Irritation and redness develop

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

Press pump twice to dever two s quits of product on to the pam of your hand
Rub hands together and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

May discolor fabrics or surfaces
Store below 110°F(43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cellulosico-polymer, zinc pyrithione

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75209-011-01 250ml 75209-011-01 250ml75209-011-01 250ml

75209-011-02 2000ml

75209-011-02 2000ml75209-011-02 2000ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2471306ethanol 94 % Topical GelPSN1
2471306ethanol 0.94 ML/ML Topical GelSCD1
2471306ethanol 94 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130872320005856GTIN-13: 0872320005856
EAN-13: 0872320005856
GTIN-12: 872320005856
UPC-A: 872320005856
GTIN storage (14 digits): 00872320005856		75209-011-01 250ml.jpg
BarcodeEAN-130872320005863GTIN-13: 0872320005863
EAN-13: 0872320005863
GTIN-12: 872320005863
UPC-A: 872320005863
GTIN storage (14 digits): 00872320005863		75209-011-02 2000ml.jpg
QR code linkQR Codecaogroup.com/75209-011-01 250ml.jpg, 75209-011-02 2000ml.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75209-011-012022-01-28C16284748780-1d6a99b39-b5b5-a426-e053-dadaa90af4c275209-011 ZAPRO HAND SANITIZER
75209-011-022022-01-28C16284748780-1d6a99b39-b5b5-a426-e053-dadaa90af4c275209-011 ZAPRO HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75209-011-01ZAPRO HAND SANITIZER250 mL in 1 BOTTLEGEL2501
75209-011-02ZAPRO HAND SANITIZER2000 mL in 1 BOTTLEGEL20001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75209-011ZAPRO HAND SANITIZER (HAND SANITIZER) GEL [GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.]1Legacy NDC, 2 package rows20201226_b75ad59f-a0f2-f861-e053-2995a90af4e4.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
75209-01175209-011-01, 75209-011-02

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
PYRITHIONE ZINCR953O2RHZ5IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
POWDERED CELLULOSESMD1X3XO9MIACT

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
b75ad59f-a0f1-f861-e053-2995a90af4e4b75ad59f-a0f2-f861-e053-2995a90af4e42020-12-26WarningsExact identifier
spl id: b75ad59f-a0f1-f861-e053-2995a90af4e4
spl set id: b75ad59f-a0f2-f861-e053-2995a90af4e4

Reported adverse events (FAERS/openFDA)#

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