ELEPBABY DISINFECTANT- spray disinfectant liquid

elepbaby disinfectant by

Drug Labeling and Warnings

elepbaby disinfectant by is a Otc medication manufactured, distributed, or labeled by Suzhou Nagongfang Health Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Modified povidone iodine 0.08-0.3%
plant extract germicidal extract 0.1%

INACTIVE INGREDIENT

medical purified water
nano-surfactant

INDICATIONS & USAGE

1、Use without dilution, direct spraying, 5- 10ml per square meter, 60 seconds after the completion of sterilization.
2、Spray after natural air drying, do not immediately dry water, otherwise it will reduce the disinfection effect.
3、To metal utensils, tableware, fruits, vegetables disinfection, can be directly soaked with this product,soaked for three minutes with water rinse clean.
4、Clean fibers, fur products, clothing, closets and cupboards before spraying, and repeat the spray every 3 hours for better results.
5、When disinfecting the pet, please put a good muzzle on the pet to avoid excessive licking.

PURPOSE

Disinfection
Sterilization
No Rinseing

WARNINGS

keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children

DOSAGE & ADMINISTRATION

It can be pressed for 2-3 times during use, can spray directly on the skin and the surface of the object without drying, and can complete disinfection and sterilization of the hand within 30-60 seconds.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ELEPBABY DISINFECTANT 
spray disinfectant liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41506-002
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	7.7 mg  in 500 mL

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

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code	elepbaby
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41506-002-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/08/2020

Labeler - Suzhou Nagongfang Health Technology Co., Ltd. (415062362)

Establishment
Name	Address	ID/FEI	Business Operations
Suzhou Nagongfang Health Technology Co., Ltd.		415062362	manufacture(41506-002)