Home NDC 24286-1528 De La Cruz Tincture of Iodine
Product NDC 24286-1528
11-digit product format 242861528
Labeler code 24286
Product ID 24286-1528_0c940d4f-cca2-7175-e063-6394a90af568
Type HUMAN OTC DRUG
Nonproprietary name Iodine and Sodium Iodide and Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler DLC Laboratories, Inc.
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 De La Cruz Tincture of Iodine
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 24286-1528-7 De La Cruz Tincture of Iodine 30 mL in 1 BOTTLE LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24286-1528 DE LA CRUZ TINCTURE OF IODINE (IODINE AND SODIUM IODIDE AND ALCOHOL) LIQUID [DLC LABORATORIES, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20231216_5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b.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 100 of 114 · 2,275 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 24286-1528-7 24286152807 30 mL in 1 BOTTLE (24286-1528-7) 30 ml 2017-10-27 0000-00-00 No No Current