VAXOL PURI- phenoxyethanol liquid 
OPENKOREA CO., Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active Ingredient

Phenoxyethanol 1.5%

Purpose

Antiseptic

Use

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

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

On open skin wounds, Do not drink.

When using this product

If it gets into your eyes Rinse immediately with water.

Ask Doctor

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

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

Directions

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

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

Package Label

50ml VAXOL PURI 81268-201-01

VAXOL PURI 
phenoxyethanol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81268-201
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T) (PHENOXYETHANOL - UNII:HIE492ZZ3T) PHENOXYETHANOL1.5 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
.GAMMA.-TERPINENE (UNII: 4YGF4PQP49)  
WATER (UNII: 059QF0KO0R)  
P-CYMENE (UNII: 1G1C8T1N7Q)  
HEXANEDIOL (UNII: ZIA319275I)  
.ALPHA.-PINENE (UNII: JPF3YI7O34)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81268-201-0150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
2NDC:81268-201-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
3NDC:81268-201-032000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/17/2020
Labeler - OPENKOREA CO., Ltd (695742727)
Registrant - OPENKOREA CO., Ltd (695742727)
Establishment
NameAddressID/FEIBusiness Operations
OPENKOREA CO., Ltd695742727manufacture(81268-201)

Revised: 11/2021
Document Id: d108fd0e-3bd5-3535-e053-2a95a90a9b08
Set id: b6a13a8c-2d15-7b31-e053-2995a90ab890
Version: 2
Effective Time: 20211117
 
OPENKOREA CO., Ltd