NAOCLEAN E-WATER- sodium hypochlorite liquid

NaOClean E-Water by

Drug Labeling and Warnings

NaOClean E-Water by is a Otc medication manufactured, distributed, or labeled by D&D Electronics Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium hypochlorite

PURPOSE

For disinfecting to remove bacteria

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

● Shake thoroughly before use.

● Without mixing any other ingredients or diluting with water, spray towards the intended area and/or objects.

● Store in a cool place away from direct sunlight

WARNINGS

● Do not drink as it is not intended for drinking.

● Do not immerse or spray for kitchen knives, aluminum containers, etc. as corrosion may occur.

● Be careful of discoloration of colored clothes.

● Do not leave for a long time in heat or ultraviolet rays as lower sterilization.

● Do not use for any other purpose. (For external use only.)

● Avoid contact with eyes. If contact occurs, flush with water.

● Stop use and ask doctor if, in rare instances, redness and irritation develop and persists for more than 72 hours.

● Keep out of reach of children. If swallowed, contact a physician.

DOSAGE & ADMINISTRATION

for external use only

INACTIVE INGREDIENT

water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NAOCLEAN E-WATER 
sodium hypochlorite liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76876-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N)	SODIUM HYPOCHLORITE	0.02 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76876-0002-1	20000 mL in 1 CONTAINER; Type 0: Not a Combination Product	08/08/2020

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

Labeler - D&D Electronics Co Ltd (557825263)

Registrant - D&D Electronics Co Ltd (557825263)

Establishment
Name	Address	ID/FEI	Business Operations
D&D Electronics Co Ltd		695625894	manufacture(76876-0002)