Active Ingredient
Phenoxyethanol 1.5%
Vaxol Puri
FDA Label NDC 81268-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Openkorea Co., Ltd for the product Vaxol Puri (NDC 81268-201). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, when using this product, ask doctor, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
* Please review the disclaimer below.
