VAXOL PURI

Manufacturer
OPENKOREA CO., Ltd
Effective date
2021-11-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:44:59

Label at a glance#

ProductVAXOL PURI
Active ingredientPHENOXYETHANOL
Label structure11 sections

Dosage and administration

Spray on a target that requires sterilization and deodorization, Use for air sterilization in crowded places, Use for children's supplies, toys and clothing, Use in stinking or unsanitary spaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Phenoxyethanol 1.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

DOSAGE & ADMINISTRATION SECTION

For use on clothing or people, Spray it at home, at school, at the office, Stores and spaces with a large floating population, Target requiring sterilization and deodorization.

Warnings

WARNINGS SECTION

Check the label before use, Do not throw or drop, People with damaged skin should be careful not to come into contact for a long time, Don't drink.

Do not use

OTC - DO NOT USE SECTION

On open skin wounds, Do not drink.

When using this product

OTC - WHEN USING SECTION

If it gets into your eyes Rinse immediately with water.

Ask Doctor

OTC - ASK DOCTOR SECTION

If skin irritation or red spots appear, seek medical treatment. If you eat or swallow, take first aid and consult your doctor immediately.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Be careful not to put it in your child's mouth.

Directions

INDICATIONS & USAGE SECTION

Spray on a target that requires sterilization and deodorization, Use for air sterilization in crowded places, Use for children's supplies, toys and clothing, Use in stinking or unsanitary spaces.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified Water, Hexanediol, d-Limonene, alpha-Pinene, gamma-Terpinene, para-Cymene

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50ml VAXOL PURI 81268-201-0150ml VAXOL PURI 81268-201-01

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81268-201-01VAXOL PURI50 mL in 1 BOTTLE, SPRAYLIQUID502
81268-201-02VAXOL PURI500 mL in 1 BOTTLE, SPRAYLIQUID5002
81268-201-03VAXOL PURI2000 mL in 1 BOTTLE, PLASTICLIQUID20002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81268-201VAXOL PURI (PHENOXYETHANOL) LIQUID [OPENKOREA CO., LTD]2Legacy NDC, 3 package rows20211119_b6a13a8c-2d15-7b31-e053-2995a90ab890.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
81268-20181268-201-01, 81268-201-02, 81268-201-03

Ingredients#

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

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

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
d108fd0e-3bd5-3535-e053-2a95a90a9b08b6a13a8c-2d15-7b31-e053-2995a90ab8902021-11-17WarningsExact identifier
spl id: d108fd0e-3bd5-3535-e053-2a95a90a9b08
spl set id: b6a13a8c-2d15-7b31-e053-2995a90ab890

Reported adverse events (FAERS/openFDA)#

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