Home NDC 63868-330 Quality Choice Iodine Tincture Mild
Product NDC 63868-330
11-digit product format 638680330
Labeler code 63868
Product ID 63868-330_0cf49a57-812c-2985-e063-6294a90aa887
Type HUMAN OTC DRUG
Nonproprietary name Iodine and Sodium Iodide and Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Chain Drug Market Association
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 1979-01-01
Substance IODINE; SODIUM IODIDE; ALCOHOL
Active strength 20; 20.4; 470 mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Quality Choice Iodine Tincture Mild
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IODINE 20 mg/mL SODIUM IODIDE 20.4 mg/mL ALCOHOL 470 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 F5WR8N145C Internal UNII lookup 3K9958V90M 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 63868-330-01 Quality Choice Iodine Tincture Mild 30 mL in 1 BOTTLE LIQUID 30 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63868-330 QUALITY CHOICE IODINE TINCTURE MILD (IODINE AND SODIUM IODIDE AND ALCOHOL) LIQUID [CHAIN DRUG MARKET ASSOCIATION] 5 Current NDC, Legacy NDC, 1 package rows 20231221_55c970ed-13a9-4ea2-a8cb-aaf14d3a214d.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 105 of 114 · 2,270 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63868-330-01 63868033001 30 mL in 1 BOTTLE (63868-330-01) 30 ml 2017-12-12 0000-00-00 No No Current