Sunmark Iodine
Sunmark Iodine is an FDA drug label for the active ingredient IODINE, SODIUM IODIDE, ALCOHOL manufactured by Strategic Sourcing Services LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231219.
Generic: IODINE, SODIUM IODIDE, ALCOHOL
Manufacturer: Strategic Sourcing Services LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 49348-133
Application: M003
Effective: 20231219
Active Ingredients: Active Ingredients Iodine 2%, Sodium Iodide 2.4%, Alcohol 47%
Indications & Usage
Uses To help prevent infection in minor cuts, scrapes and burns.
Dosage & Administration
DIRECTIONS: Clean the affected area. Apply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.
Contraindications
Not available.
Warnings
WARNINGS: For external use only.
Adverse Reactions
Not available.
More from same ingredient
No related products.