NDC 29983-1061 - Icon Imperial NPE Free

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 29983-1061
Package NDCs from labels: 29983-1061-8, 29983-1061-9
Manufacturer: IBA | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date: 2025-12-02
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Icon Imperial NPE Free	IBA \| Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	2025-12-02	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
29983-1061-8	Icon Imperial NPE Free	231.26 kg in 1 DRUM	LIQUID	231.26		11
29983-1061-9	Icon Imperial NPE Free	1156.31 kg in 1 CONTAINER	LIQUID	1156.31		11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
29983-1061	ICON IMPERIAL NPE FREE (IODINE) LIQUID [IBA]	10	2 package rows	20241108_a8d2dfa7-0cdd-40cf-9fae-6b0c6708109b.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 12 of 12 · 222 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bio Iodine	IODIUM	BioActive Nutritional, Inc.	69be0ca4-99b7-4de0-b4f2-5723b1f1a7da	2016-08-11	Warnings	Exact identifier unii: 9679TC07X4
Thyrotox	CHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEA	BioActive Nutritional, Inc.	e229a260-13f3-4136-b325-9a8954f8a327	2016-08-10	Warnings	Exact identifier unii: 9679TC07X4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.