PROVTECT HAND SANITIZER- chlorine dioxide spray 
Ignal

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

Chlorine Dioxide 0.01%

INACTIVE INGREDIENT

Water

PURPOSE

Antimicrobial

WARNINGS

For external use only. Avoid direct sunlight and store in a cool place.
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Do not use
• in children less than 2 months of age
• internal wound • inhalation by fumigation
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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Keep out of reach of children. If nauseous feeling or sickness occurs, when swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

If nauseous feeling or sickness occurs, when swallowed, get medical help or contact a Poison Control Center right away.

Uses

■ Hand Sanitizer help to reduce germs and inactivate viruses that potentially can cause disease.

Directions

■ Spray on or Wet palms, rub hands thoroughly together until dry.
■ Supervise children under 6.

Other information

■ Store between 5-20C (41-68F)
■ Avoid freezing and excessive heat above 40C (104F)

Questions?

Questions 8231-717-2562
www.ignal.co.kr
ignal.co.kr@gmail.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

PROVTECT HAND SANITIZER 
chlorine dioxide spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81754-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Chlorine Dioxide (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) Chlorine Dioxide0.05 g  in 500 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81754-010-01500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/2021
Labeler - Ignal (695036204)
Registrant - Ignal (695036204)
Establishment
NameAddressID/FEIBusiness Operations
Ignal695036204manufacture(81754-010)

Revised: 4/2021
Document Id: ad0b6b26-fd75-43f1-b507-6bdbaab53bde
Set id: cb405d24-45a5-40ce-8328-9a6cfb4b6ad9
Version: 1
Effective Time: 20210408
 
Ignal