Home NDC 48433-230-15 Strong Iodine Solution
Product NDC 48433-230
Requested package NDC 48433-230-15
11-digit product format 484330230
Labeler code 48433
Product ID 48433-230_3d1d89c5-85de-4aa8-9145-5ec6a25983ce
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Strong Iodine Solution
Dosage form SOLUTION/ DROPS
Route ORAL
Labeler Safecor Health, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2008-09-20
Substance IODINE; POTASSIUM IODIDE
Active strength 700; 1400 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 Strong Iodine Solution
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IODINE 700 mg/mL POTASSIUM IODIDE 1400 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9679TC07X4 Internal UNII lookup 1C4QK22F9J Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 204913 Internal RxNorm 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 48433-230-15 Strong Iodine Solution 14 mL in 1 BOTTLE SOLUTION/ DROPS 14 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48433-230 STRONG IODINE SOLUTION SOLUTION/ DROPS [SAFECOR HEALTH, LLC] 3 Current NDC, Legacy NDC, 1 package rows 20250110_ec12b0ab-8fee-4b4f-a6e7-349f60a6f3e0.zip
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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48433-230-15 48433023015 14 mL in 1 BOTTLE (48433-230-15) 14 ml 2008-09-20 0000-00-00 No No Current