FDA.reportPublic FDA data

Pube Chlorine Dioxide Disinfection

Manufacturer
Guangdong Jiajie Technology Co., Ltd.
Effective date
2024-01-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:06:40

Label at a glance#

ProductPube Chlorine Dioxide Disinfection
Active ingredientSODIUM CHLORITE
Label structure11 sections

Dosage and administration

Dissolve 1g of product into 1 Liter of purified water to generate 50mg -100mg of Chlorine Dioxide.

Storage and handling

Please follow the instructions in the user manual.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Sodium Chlorite 30.0%

Purpose

OTC - PURPOSE SECTION

Disinfection.

Use

INDICATIONS & USAGE SECTION

For external use only.

Warnings

WARNINGS SECTION

Keep away from direct sunlight.
For external use only.

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

/

Directions

DOSAGE & ADMINISTRATION SECTION

Dissolve 1g of product into 1 Liter of purified water to generate 50mg -100mg of Chlorine Dioxide.

Other information

STORAGE AND HANDLING SECTION

Please follow the instructions in the user manual.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium Carbonate, Anhydrous Sodium Sulfate,Citric Acid,Sodium Chloride,Boric Acid,Corn Starch.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

User Manual

User ManualUser Manual

81391-001-01 Outer packaging

81391-001-01 Outer packaging81391-001-01 Outer packaging

81391-001-11 inner packaging

81391-001-11 inner packaging81391-001-11 inner packaging

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81391-001-012025-07-29C16284748780-13b156c62-2def-fb37-e063-e6dba90a4e0781391-001 Meeting Zhuoma Tibetan Medicine YO Nano Superconducting Disinfection Factor Pube Chlorine Dioxide Disinfection Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81391-001-01Pube Chlorine Dioxide Disinfection10 in 1 BAGTABLET105
81391-001-11Pube Chlorine Dioxide Disinfection1 g in 1 POUCHTABLET15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81391-001PUBE CHLORINE DIOXIDE DISINFECTION (PUBE CHLORINE DIOXIDE DISINFECTION TABLETS) TABLET [GUANGDONG JIAJIE TECHNOLOGY CO., LTD.]5Legacy NDC, 2 package rows20240105_b84a7312-cbe6-3899-e053-2995a90a285c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81391-00181391-001-11, 81391-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
STARCH, CORNO8232NY3SJIACT
BORIC ACIDR57ZHV85D4IACT
SODIUM SULFATE ANHYDROUS36KCS0R750IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CARBONATE45P3261C7TIACT
SODIUM CHLORITEG538EBV4VFACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0e1adb2e-a3aa-d37d-e063-6394a90ab743b84a7312-cbe6-3899-e053-2995a90a285c2024-01-04WarningsExact identifier
spl id: 0e1adb2e-a3aa-d37d-e063-6394a90ab743
spl set id: b84a7312-cbe6-3899-e053-2995a90a285c

Reported adverse events (FAERS/openFDA)#

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