Active Ingredient(S)
Sodium Chlorite 30.0%
Pube Chlorine Dioxide Disinfection
FDA Label NDC 81391-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Jiajie Technology Co., Ltd. for the product Pube Chlorine Dioxide Disinfection (NDC 81391-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Disinfection.
Use
For external use only.
Warnings
Keep away from direct sunlight.
For external use only.
Do Not Use
/
Otc - When Using
/
Otc - Stop Use
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Directions
Dissolve 1g of product into 1 Liter of purified water to generate 50mg -100mg of Chlorine Dioxide.
Other Information
Please follow the instructions in the user manual.
Inactive Ingredients
Sodium Carbonate, Anhydrous Sodium Sulfate,Citric Acid,Sodium Chloride,Boric Acid,Corn Starch.
Package Label - Principal Display Panel
User Manual
81391-001-01 Outer packaging
81391-001-11 inner packaging
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