Otc - Active Ingredient
potassium carbonate
Zeroq
FDA Label NDC 80643-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jisang Co., Ltd. for the product Zeroq (NDC 80643-0001). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
e-polylysine, dextrin, 1,2-propanediol, citric acid, tea catechin, hydroxypropylmethyl cellulose, water
Otc - Purpose
Sanitizer to help decrease bacteria on skin
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Spray on skin as needed
Warnings
For external use only.
When using this product
Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Store at room temperature.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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