KO-C100- chlorine dioxide tablet, for solution

KO-C100 by

Drug Labeling and Warnings

KO-C100 by is a Otc medication manufactured, distributed, or labeled by DONG FUH BIOTECH CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Chlorine Dioxide 0.1g/1g. Purpose: Sterilization, disinfection

Purpose

Sterilization, disinfection

Use(s)

It is suitable for environmental disinfection in public spaces, public transportation, schools, hospitals, stores, restaurants, homes, food factories, and animal husbandry.

Warnings

External Use Only. Do not take orally.

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

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.

STOP USE

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

Keep out of the reach of children.

Directions

Take out 1 KO-100C Disinfectant, add it to a container filled with 1000c.c. water, let it stand for 1-3 minutes to dissolve into a light yellow disinfectant stock solution, and then distribute it to various containers for immediate use.

Other information

• Store at a cool place
• Valid period: 2 years

Inactive ingredients

Citric Acid, Magnesium Sulfate, Sodium Bicarbonate, Sodium Chloride

Package Label - Principal Display Panel

1g * 1000 tablet, NDC: 81797-701-13

INGREDIENTS AND APPEARANCE

KO-C100 
chlorine dioxide tablet, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81797-701
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM)	CHLORINE DIOXIDE	0.1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Product Characteristics
Color	yellow	Score	no score
Shape	ROUND	Size	10mm
Flavor	EGG NOG	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81797-701-15	1000 in 1 PACKAGE	04/09/2021
1	NDC: 81797-701-00	1 g in 1 DOSE PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/09/2021

Labeler - DONG FUH BIOTECH CO., LTD. (658813795)

Establishment
Name	Address	ID/FEI	Business Operations
DONG FUH BIOTECH CO., LTD.		658813795	manufacture(81797-701)