Active Ingredient
Povidone-iodine USP 10%
10% Povidone Iodine Nasal Swab
FDA Label NDC 83062-497
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Iimed Medical Mexicana S De Rl De Cv for the product 10% Povidone Iodine Nasal Swab (NDC 83062-497). 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, purpose, uses, warnings, do not use, ask a doctor before use if injuries are, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- • antiseptic skin preparation
- • helps reduce bacteria that can potentially cause skin infections
Warnings
For external use only
Do Not Use
- • if allergic to iodine
- • in the eyes
- • on children less than 3 years old
Ask A Doctor Before Use If Injuries Are
- • deep or puncture wounds
- • serious burns
Stop Use And Ask A Doctor If
- • redness, irritation, swelling or pain persists or increases
- • infection occurs
Keep Out Of Reach Of Children.
In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.
Storage And Handling
Avoid excessive heat.Store at room temperature.
Directions
NASAL APPLICATION:
 Figure (Clorox 01) |
|
 Figure (Clorox 02) |
|
 Figure (Clorox 03) |
|
 Figure (Clorox 04) |
|
 Figure (Clorox 05) |
|
Other Information
- • 1% titratable iodine
- • not made with natural rubber latex
- • for hospital or professional use only
Inactive Ingredients
disodium phosphate, glycerin, hydroxyethylcellulose, nonoxynol-10, simethicone, water
Package Label
* Please review the disclaimer below.
