Home NDC 69452-484 mild iodine tincture
Product NDC 69452-484
11-digit product format 694520484
Labeler code 69452
Product ID 69452-484_3ed930e0-0e74-277b-e063-6394a90a1b31
Type HUMAN OTC DRUG
Nonproprietary name Iodine and Sodium Iodide and Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler BIONPHARMA INC.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-06
Substance IODINE; ALCOHOL; SODIUM IODIDE
Active strength 20; 470; 20.4 mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base mild iodine tincture
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IODINE 20 mg/mL ALCOHOL 470 mg/mL SODIUM IODIDE 20.4 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9679TC07X4 Internal UNII lookup 3K9958V90M Internal UNII lookup F5WR8N145C Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69452-484-36 mild iodine tincture 30 mL in 1 BOTTLE LIQUID 30 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 44 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69452-484-36 69452048436 30 mL in 1 BOTTLE (69452-484-36) 30 ml 2025-10-06 No No Current