Otc - Active Ingredient
Active Ingredient: Povidone-Iodine USP (10%)
Povidone Iodine Prep Pad Solution
FDA Label NDC 73288-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Tianbo First Aid Product Co., Ltd. for the product Povidone Iodine Prep Pad (NDC 73288-002). 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, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, otc - ask doctor, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antiseptic
Indications & Usage
Use:
First aid antiseptic to help prevent infection in minor cuts, scrapes and burns.
Warnings
Warnings:
For external use only
Do not use if allergic to iodine or in the eyes
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately
Otc - Ask Doctor
Stop use and ask a doctor if infection occurs or if redness, irritation, swelling, or pain persists or increases
Dosage & Administration
Apply locally as need
Inactive Ingredient
Inactive Ingredient
Citric acid, purified water, Sodium phosphate dibasic
Package Label.Principal Display Panel
Image Description (Iodine)
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