Home NDC 66096-166-02 Kali Iodatum 1X
Product NDC 66096-166
Requested package NDC 66096-166-02
11-digit product format 660960166
Labeler code 66096
Product ID 66096-166_d44b323b-080a-b3d4-e053-2995a90aafb7
Type HUMAN OTC DRUG
Nonproprietary name Kali Iodatum.
Dosage form LIQUID
Route ORAL
Labeler OHM PHARMA INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-02-10
Substance POTASSIUM IODIDE
Active strength 1 [hp_X]/30mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Kali Iodatum 1X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM IODIDE 1 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1C4QK22F9J Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66096-166-02 Kali Iodatum 1X 30 mL in 1 BOTTLE, DROPPER LIQUID 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66096-166 KALI IODATUM 1X (KALI IODATUM.) LIQUID [OHM PHARMA INC.] 4 Current NDC, Legacy NDC, 1 package rows 20211230_682a651b-699d-45c6-8161-4b802cda1d7d.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 66096-166-02 66096016602 30 mL in 1 BOTTLE, DROPPER (66096-166-02) 30 ml 2016-02-10 0000-00-00 No No Current