OKGO Disinfectant

Manufacturer
Henan Seagood Medical Equipment Co., Ltd.
Effective date
2021-01-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:23

Label at a glance#

ProductOKGO Disinfectant
Active ingredientDIDECYLDIMONIUM CHLORIDE
Label structure13 sections

Dosage and administration

Spray on the surface of human skin and let it dry naturally. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

OKGO®Disinfectant

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Didecyl dimethyl ammonium chloride 0.5g/L. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

OKGO®Disinfectant to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only.

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray on the surface of human skin and let it dry naturally.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Fatty alcohol polyoxyethylene ether
Dimethyldioctylammonium chloride
Dodecyldimethylbenzylammonium chloride
Benzyldimethylhexadecylammonium chloride
essence
water
Alkyl indican
triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81476-101-01OKGO Disinfectant30 mL in 1 BOTTLESPRAY301
81476-101-02OKGO Disinfectant50 mL in 1 BOTTLESPRAY501
81476-101-03OKGO Disinfectant100 mL in 1 BOTTLESPRAY1001
81476-101-04OKGO Disinfectant450 mL in 1 BOTTLESPRAY4501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81476-101OKGO DISINFECTANT (DIDECYL DIMETHYL AMMONIUM CHLORIDE) SPRAY [HENAN SEAGOOD MEDICAL EQUIPMENT CO., LTD.]1Legacy NDC, 4 package rows20210127_b9c5d0c4-7897-60fa-e053-2a95a90a7909.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81476-10181476-101-01, 81476-101-02, 81476-101-03, 81476-101-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
b9c5d0c4-7889-60fa-e053-2a95a90a7909b9c5d0c4-7897-60fa-e053-2a95a90a79092021-01-25WarningsExact identifier
spl id: b9c5d0c4-7889-60fa-e053-2a95a90a7909
spl set id: b9c5d0c4-7897-60fa-e053-2a95a90a7909

Reported adverse events (FAERS/openFDA)#

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