OKGO DISINFECTANT- didecyl dimethyl ammonium chloride spray

OKGO Disinfectant by

Drug Labeling and Warnings

OKGO Disinfectant by is a Otc medication manufactured, distributed, or labeled by Henan Seagood Medical Equipment Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

OKGO®Disinfectant

Active Ingredient(s)

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

Purpose

Antiseptic

Use

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

Warnings

For external use only.

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

Directions

• 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

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

Inactive ingredients

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

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

OKGO DISINFECTANT 
didecyl dimethyl ammonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81476-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM CHLORIDE	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM (UNII: 7N6JUD5X6Y)
(C10-C16)ALKYLDIMETHYLAMINE OXIDE (UNII: LF6BKC321J)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
DIOCTYLDIMONIUM CHLORIDE (UNII: 0X0RL40Y6H)
WATER (UNII: 059QF0KO0R)
METHYL BENZOATE (UNII: 6618K1VJ9T)
TROLAMINE (UNII: 9O3K93S3TK)
STEARALKONIUM CHLORIDE (UNII: 0OUO26BB88)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81476-101-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/26/2021
2	NDC: 81476-101-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/26/2021
3	NDC: 81476-101-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/26/2021
4	NDC: 81476-101-04	450 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/26/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/26/2021

Labeler - Henan Seagood Medical Equipment Co., Ltd. (715343285)

Establishment
Name	Address	ID/FEI	Business Operations
Henan Seagood Medical Equipment Co., Ltd.		715343285	manufacture(81476-101)