AV-1000- sodium chlorite, citric cid powder

AV-1000 by

Drug Labeling and Warnings

AV-1000 by is a Otc medication manufactured, distributed, or labeled by Sejin E&P Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

sodium chlorite 0.05%

citric acid 0.06%

INACTIVE INGREDIENT

magnesium silicate, aluminum silicate, rheology modifier

PURPOSE

for objects to sterilize virus, vacteria and fungi etc.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

This product can not be eaten. And do not use it for other purposes

Avoid using in places exposed to high temperatures and direct sunlight for prolonged periods of time.

Put or Inserted in employee ID case, handbag, wallet, pocket or mask storage case.

WARNINGS

For objects use only

If you feel irritation in an enclosed space, provide enough ventilation

If the product comes into contact with the skin for a long time, itching may be caused.
Wash it thoroughly with running water and immediately consult a doctor if there is any abnormality.

DOSAGE & ADMINISTRATION

For objects use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AV-1000 
sodium chlorite, citric cid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77130-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL)	ANHYDROUS CITRIC ACID	0.06 g  in 100 g
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	0.05 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM SILICATE (UNII: 9B9691B2N9)
ALUMINUM SILICATE (UNII: T1FAD4SS2M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77130-0001-1	8 g in 1 PACKAGE; Type 0: Not a Combination Product	05/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/02/2020

Labeler - Sejin E&P Co., Ltd. (694459360)

Registrant - Sejin E&P Co., Ltd. (694459360)

Establishment
Name	Address	ID/FEI	Business Operations
Sejin E&P Co., Ltd.		694459360	manufacture(77130-0001)