SSKI

Product NDC: 71740-112
11-digit product format: 717400112
Labeler code: 71740
Product ID: 71740-112_6a232f5f-b029-4908-98b1-eda6ab98f451
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Potassium Iodide
Dosage form: SOLUTION
Route: ORAL
Labeler: Avondale Pharmaceuticals, LLC
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	71740-112	71740-112-08	D	Discontinued by firm		2026-08-11

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 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
312541	Internal RxNorm lookup
544597	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
ca1d3449-ea29-49a4-8863-365ec95f1553	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
4073022c-5d5d-48f5-82ed-091ad146a4b2	Product name	1	20171211
9ffbd0ae-0bce-c086-b707-f0da5f8cd7c5	Product name	1	20150828

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71740-112-08	SSKI	1 in 1 CARTON	SOLUTION	1	7
71740-112-08	SSKI	237 mL in 1 BOTTLE	SOLUTION	237	7
71740-112-30	SSKI	30 mL in 1 BOTTLE, WITH APPLICATOR	SOLUTION	30	7
71740-112-30	SSKI	1 in 1 CARTON	SOLUTION	1	7

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71740-112-08	ML - Milliliter	71740-112	aacc6625-4b13-4238-8f92-441e389b4809	1	2017-12-14
71740-112-30	ML - Milliliter	71740-112	9a15cfe6-bc92-45fb-85e3-e1fe8fafe529	1	2017-12-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71740-112	SSKI (POTASSIUM IODIDE) SOLUTION [AVONDALE PHARMACEUTICALS, LLC]	6	Current NDC, Legacy NDC, 4 package rows	20240125_ca1d3449-ea29-49a4-8863-365ec95f1553.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	Avondale Pharmaceuticals, LLC	ca1d3449-ea29-49a4-8863-365ec95f1553	2025-07-09	Warnings, Adverse reactions	Exact identifier ndc (product): 71740-112

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
1C4QK22F9J	POTASSIUM IODIDE	7681-11-0	POTASSIUM IODIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312541	potassium iodide 1 GM in 1 mL Oral Solution	PSN	ca1d3449-ea29-49a4-8863-365ec95f1553	7
544597	SSKI 1 GM in 1 mL Oral Solution	PSN	ca1d3449-ea29-49a4-8863-365ec95f1553	7
544597	potassium iodide 1000 MG/ML Oral Solution [SSKI brand of Potassium Iodide]	SBD	ca1d3449-ea29-49a4-8863-365ec95f1553	7
312541	potassium iodide 1000 MG/ML Oral Solution	SCD	ca1d3449-ea29-49a4-8863-365ec95f1553	7
312541	K+ Iodide 1000 MG/ML Oral Solution	SY	ca1d3449-ea29-49a4-8863-365ec95f1553	7
544597	K+ Iodide 1000 MG/ML Oral Solution [SSKI brand of Potassium Iodide]	SY	ca1d3449-ea29-49a4-8863-365ec95f1553	7
312541	Pot Iodide 1000 MG/ML Oral Solution	SY	ca1d3449-ea29-49a4-8863-365ec95f1553	7
544597	Pot Iodide 1000 MG/ML Oral Solution [SSKI brand of Potassium Iodide]	SY	ca1d3449-ea29-49a4-8863-365ec95f1553	7
312541	potassium iodide 1 GM per 1 ML Oral Solution	SY	ca1d3449-ea29-49a4-8863-365ec95f1553	7
544597	SSKI 1 GM per 1 ML Oral Solution	SY	ca1d3449-ea29-49a4-8863-365ec95f1553	7
544597	SSKI brand of Potassium Iodide 1 GM per 1 ML Oral Solution	SY	ca1d3449-ea29-49a4-8863-365ec95f1553	7
312541	potassium iodide 1 GM in 1 mL Oral Solution	PSN	664e6cd9-6a3c-49ef-a7b2-d09f0338b549	5
312541	potassium iodide 1000 MG/ML Oral Solution	SCD	664e6cd9-6a3c-49ef-a7b2-d09f0338b549	5
312541	K+ Iodide 1000 MG/ML Oral Solution	SY	664e6cd9-6a3c-49ef-a7b2-d09f0338b549	5
312541	Pot Iodide 1000 MG/ML Oral Solution	SY	664e6cd9-6a3c-49ef-a7b2-d09f0338b549	5
312541	potassium iodide 1 GM per 1 ML Oral Solution	SY	664e6cd9-6a3c-49ef-a7b2-d09f0338b549	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71740-112-08	71740011208	1 BOTTLE in 1 CARTON (71740-112-08) > 237 mL in 1 BOTTLE	1 bottle	2017-11-13	0000-00-00	No	No	Current
71740-112-30	71740011230	1 BOTTLE, WITH APPLICATOR in 1 CARTON (71740-112-30) / 30 mL in 1 BOTTLE, WITH APPLICATOR		2017-11-13	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL	Avondale Pharmaceuticals, LLC	2025-07-09	HUMAN PRESCRIPTION DRUG LABEL	7
Potassium Iodide Oral Solution SSKI ® Potassium Iodide Oral Solution, USP (Saturated) 1 g/mL	ATLANTIC BIOLOGICALS CORP.	2025-05-28	HUMAN PRESCRIPTION DRUG LABEL	5