PROVTECT HAND SANITIZER- chlorine dioxide spray

ProVtect Hand Sanitizer by

Drug Labeling and Warnings

ProVtect Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ignal. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

PROVTECT HAND SANITIZER 
chlorine dioxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81754-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chlorine Dioxide (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM)	Chlorine Dioxide	0.05 g  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81754-010-01	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2021

Labeler - Ignal (695036204)

Registrant - Ignal (695036204)

Establishment
Name	Address	ID/FEI	Business Operations
Ignal		695036204	manufacture(81754-010)