ONTREE LIFE- chlorine dioxide, anatase liquid

ONTREE LIFE by

Drug Labeling and Warnings

ONTREE LIFE by is a Otc medication manufactured, distributed, or labeled by O2. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Chlorine dioxide 0.02%

Anatase 0.05%

Purpose

Antiseptic

Use

Medical facilities, schools, and businesses, group catering facilities, food service facilities sterilization, furniture, refrigerators, toilets

Warnings

Do not use other than the purpose of the product../ Keep in a cool place away from direct sunlight in children less than 2 months of age / on open skin wounds

When using this product : Vomit when drinking contents and consult your doctor, / Rinse immediately when eye contact occurs

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Turn the spray nozzle to fit on / Sprinkle at a distance / when sprayed in large quantities wipe lightly with a dry towel / Sufficient ventilation required for use in confined spaces /

Supervise children under 6 year of age when using this product to avoid swallowing.

Other information

Store between 12-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive ingredient

water

Package Label

INGREDIENTS AND APPEARANCE

ONTREE LIFE 
chlorine dioxide, anatase liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90105-202
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM)	CHLORINE DIOXIDE	0.02 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.05 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90105-202-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/04/2020

Labeler - O2 (695032447)

Registrant - O2 (695032447)

Establishment
Name	Address	ID/FEI	Business Operations
O2		695032447	manufacture(90105-202)