Sharkboby

Manufacturer: Guangzhou Ehang Electronic Co., Ltd.
Effective date: 2020-06-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:26:39

Label at a glance#

ProductSharkbody

Active ingredientSODIUM CHLORITE

Label structure9 sections

Dosage and administration

For external use only This products is suitable for people over 5 years old, children must use it under the supervision of parents.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Sodium chlorite

Purpose

OTC - PURPOSE SECTION

anti bacteria, virus, odors

Use

INDICATIONS & USAGE SECTION

please see the label attached

Warnings

WARNINGS SECTION

This product is not edible, do not bit.
This product is suitable for people over 5 years old, children must use it under the supervision of parents.
This product can not be stained with water after the function is invalid.
Drop the product in the trash can after replacement or failure.
If you accidentally eat or have eye contact, please go to hospital immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

For external use only
This products is suitable for people over 5 years old, children must use it under the supervision of parents.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium hydroxide

INDICATIONS & USAGE

RECENT MAJOR CHANGES SECTION

please see the label attached

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Sharkbody
Chlorine dioxide
SODIUM HYDROXIDE
SODIUM CHLORITE
CHLORITE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78504-002	78504-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM HYDROXIDE	55X04QC32I	IACT
SODIUM CHLORITE	G538EBV4VF	ACTIB

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
d1771e19-3ec4-c067-e053-2995a90a6bf8			a72bd492-eee8-02d5-e053-2a95a90acf8f	2021-11-23	Warnings	Exact identifier spl set id: a72bd492-eee8-02d5-e053-2a95a90acf8f

Reported adverse events (FAERS/openFDA)#

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