AV-1000

Manufacturer: Sejin E&P Co., Ltd.
Effective date: 2022-02-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:48:18

Label at a glance#

ProductAV-1000

Active ingredientCITRIC ACID MONOHYDRATE, SODIUM CHLORITE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium chlorite 0.05%

citric acid 0.06%

INACTIVE INGREDIENT SECTION

magnesium silicate, aluminum silicate, rheology modifier

OTC - PURPOSE SECTION

for objects to sterilize virus, vacteria and fungi etc.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

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 SECTION

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 SECTION

For objects use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
ANHYDROUS CITRIC ACID Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77130-0001-1	2023-07-28	C162847	48780-1	d6a99b39-70c2-a426-e053-dadaa90af4c2	Drug Facts
77130-0001-1	2022-02-17	C162847	48780-1	d6a99b39-70c2-a426-e053-dadaa90af4c2	Drug Facts
77130-0001-1	2022-01-28	C162847	48780-1	d6a99b39-70c2-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77130-0001-1	AV-1000	8 g in 1 PACKAGE	POWDER	8		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77130-0001	AV-1000 (SODIUM CHLORITE, CITRIC CID) POWDER [SEJIN E&P CO., LTD.]	2	Legacy NDC, 1 package rows	20220218_a4a0412a-68a3-c654-e053-2995a90ae024.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

AV-1000
sodium chlorite, citric cid
CITRIC ACID MONOHYDRATE
ANHYDROUS CITRIC ACID
SODIUM CHLORITE
CHLORITE ION
MAGNESIUM SILICATE
ALUMINUM SILICATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77130-0001	77130-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CITRIC ACID MONOHYDRATE	2968PHW8QP	ACTIM
SODIUM CHLORITE	G538EBV4VF	ACTIB
MAGNESIUM SILICATE	9B9691B2N9	IACT
ALUMINUM SILICATE	T1FAD4SS2M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d84128e4-0b5c-7242-e053-2995a90a1404			a4a0412a-68a3-c654-e053-2995a90ae024	2022-02-17	Warnings	Exact identifier spl id: d84128e4-0b5c-7242-e053-2995a90a1404 spl set id: a4a0412a-68a3-c654-e053-2995a90ae024

Reported adverse events (FAERS/openFDA)#

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