Home NDC 17856-0114 SSKI
Product NDC 17856-0114
11-digit product format 178560114
Labeler code 17856
Product ID 17856-0114_36341581-eb16-560d-e063-6394a90afb4a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Potassium Iodide
Dosage form SOLUTION
Route ORAL
Labeler ATLANTIC BIOLOGICALS CORP.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2017-11-13
Substance POTASSIUM IODIDE
Active strength 1 g/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 21 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 17856-0114-2 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 17856-0114-1 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 17856-0114-2 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 17856-0114-1 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 17856-0114-2 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 17856-0114-1 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 17856-0114-2 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 17856-0114-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 17856-0114-2 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 17856-0114-1 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 17856-0114-2 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 17856-0114-1 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 17856-0114-2 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 17856-0114-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base SSKI
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM IODIDE 1 g/mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312541 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 17856-0114-1 2025-03-28 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL 17856-0114-2 2025-03-28 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL 17856-0114-1 2025-01-30 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL 17856-0114-2 2025-01-30 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL 17856-0114-1 2023-08-18 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL 17856-0114-2 2023-08-18 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL 17856-0114-1 2023-01-30 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL 17856-0114-2 2023-01-30 Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17856-0114-1 SSKI 120 in 1 BOX, UNIT-DOSE SOLUTION 120 5 17856-0114-1 SSKI 0.1 mL in 1 SYRINGE SOLUTION 0.1 5 17856-0114-2 SSKI 120 in 1 BOX, UNIT-DOSE SOLUTION 120 5 17856-0114-2 SSKI 0.1 mL in 1 SYRINGE SOLUTION 0.1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17856-0114 SSKI (POTASSIUM IODIDE) SOLUTION [ATLANTIC BIOLOGICALS CORP.] 4 Current NDC, Legacy NDC, 4 package rows 20250331_664e6cd9-6a3c-49ef-a7b2-d09f0338b549.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SSKI POTASSIUM IODIDE ATLANTIC BIOLOGICALS CORP. 664e6cd9-6a3c-49ef-a7b2-d09f0338b549 2025-05-28 Warnings, Adverse reactions Exact identifier ndc (product): 17856-0114
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 17856-0114-1 17856011401 120 SYRINGE in 1 BOX, UNIT-DOSE (17856-0114-1) / .1 mL in 1 SYRINGE 120 syringe 2023-08-18 0000-00-00 No No Current 17856-0114-2 17856011402 120 SYRINGE in 1 BOX, UNIT-DOSE (17856-0114-2) / .1 mL in 1 SYRINGE 120 syringe 2023-08-18 0000-00-00 No No Current