FDA.reportPublic FDA data

OZLAB Hand Sanitizer

Manufacturer
Zhejiang Ounuo Cosmetics Co., Ltd.
Effective date
2020-05-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:02

Label at a glance#

ProductOZLAB Hand Sanitizer
Active ingredientalcohol
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient  -- Alcohol   75% (w/w)      

OTC - PURPOSE SECTION

Purpose - Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

  • To kill germs and bacteria.
  • recommended for repeated use.

WARNINGS SECTION

For external use only: hands
Flammable. Keep away from fire or flame.

When using this products, keep out of eyes.

Stop using and ask a doctor, if irritation or redness develops.

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product andd rub until dry.

INACTIVE INGREDIENT SECTION

Water (aqua), propylene glycol, Glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl Propanol, aloe barbadensis leaf extract, fragrance (parfum)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75531-010-012021-07-23C16284748780-1c7ccaba7-1e8d-fd44-e053-dadaa90aa01bDrug facts
75531-010-022021-07-23C16284748780-1c7ccaba7-1e8d-fd44-e053-dadaa90aa01bDrug facts
75531-010-032021-07-23C16284748780-1c7ccaba7-1e8d-fd44-e053-dadaa90aa01bDrug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75531-010-01OZLAB Hand Sanitizer100 mL in 1 BOTTLE, PLASTICGEL1001
75531-010-02OZLAB Hand Sanitizer250 mL in 1 BOTTLE, PLASTICGEL2501
75531-010-03OZLAB Hand Sanitizer500 mL in 1 BOTTLE, PLASTICGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75531-010OZLAB HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG OUNUO COSMETICS CO., LTD.]1Legacy NDC, 3 package rows20200529_04c0c4c1-6f69-4f97-982e-5fea91c6d203.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75531-01075531-010-01, 75531-010-02, 75531-010-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
alcohol3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
484c84a0-c1c2-42e1-b659-8bde0a580f2304c0c4c1-6f69-4f97-982e-5fea91c6d2032020-05-28WarningsExact identifier
spl id: 484c84a0-c1c2-42e1-b659-8bde0a580f23
spl set id: 04c0c4c1-6f69-4f97-982e-5fea91c6d203

Reported adverse events (FAERS/openFDA)#

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