Povidone-iodine Scrub Sterile Swab
FDA Label NDC 63517-252
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health 200, Inc for the product Povidone-iodine Scrub Sterile (NDC 63517-252). 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 drug facts, active ingredient, purpose, use, warnings, do not use, ask a doctor before use if injuries are, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Povidone-Iodine 7.5%
Purpose
Antiseptic
Use
• For preparation prior to surgery
• Helps to reduce bacteria that can potentially cause skin infection
Warnings
For external use only.
Do Not Use
• in the eyes
Ask A Doctor Before Use If Injuries Are
• deep wounds • puncture wounds • serious burns
Stop Use And Ask A Doctor If
• irritation and redness develop • condition persists for more than 72 hours • infection occurs
Avoid Pooling Beneath The Patient.
Prolonged exposure to wet solution may cause skin irritation.
Keep Out Of Reach Of Children.
If swallowed or gets in eyes, get medical help or contact a Poison Control Center right away.
Directions
Clean the area. Apply product to the operative site prior to surgery using sponge sticks to prep desired area.
Other Information
• saturating solution contains 0.75% titratable iodine • latex free • for hospital or professional use only
Inactive Ingredients
Citric Acid, Alkyl Glucoside, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified Water
Product Label
Boxlabel (Boxlabel)
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