KO-C100

Manufacturer
DONG FUH BIOTECH CO., LTD.
Effective date
2022-11-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:51:47

Label at a glance#

ProductKO-C100
Active ingredientCHLORINE DIOXIDE
Label structure12 sections

Dosage and administration

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.

Storage and handling

Store at a cool place Valid period: 2 years

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

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

Purpose

OTC - PURPOSE SECTION

Sterilization, disinfection

Use(s)

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

External Use Only. Do not take orally.

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Citric Acid, Magnesium Sulfate, Sodium Bicarbonate, Sodium Chloride

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81797-701-152024-01-30C16284748780-11030e365-1e2f-111a-e063-dadaa90a10e2DFB, KO-C100

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81797-701-00KO-C1001 g in 1 DOSE PACKTABLET, FOR SOLUTION12
81797-701-15KO-C1001000 in 1 PACKAGETABLET, FOR SOLUTION10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81797-701KO-C100 (CHLORINE DIOXIDE) TABLET, FOR SOLUTION [DONG FUH BIOTECH CO., LTD.]2Legacy NDC, 2 package rows20221123_bf823253-00ce-20d6-e053-2995a90a3fcc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81797-70181797-701-00, 81797-701-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ee0b621b-e920-635e-e053-2a95a90a5639bf823253-00ce-20d6-e053-2995a90a3fcc2022-11-23WarningsExact identifier
spl id: ee0b621b-e920-635e-e053-2a95a90a5639
spl set id: bf823253-00ce-20d6-e053-2995a90a3fcc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.