Home NDC 29983-0017 NDC 29983-0017 - ULTRA-SHIELD 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 29983-0017
Package NDCs from labels 29983-0017-1, 29983-0017-4, 29983-0017-6, 29983-0017-7, 29983-0017-8
Manufacturer IBA
Effective date 2024-12-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type ULTRA-SHIELD - IBA IBA 2024-12-31 OTC ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 29983-0017-1 ULTRA-SHIELD 3.78 L in 1 DRUM SOLUTION 3.78 3 29983-0017-4 ULTRA-SHIELD 18.9 L in 1 DRUM SOLUTION 18.9 3 29983-0017-6 ULTRA-SHIELD 56.7 L in 1 DRUM SOLUTION 56.7 3 29983-0017-7 ULTRA-SHIELD 113.4 L in 1 DRUM SOLUTION 113.4 3 29983-0017-8 ULTRA-SHIELD 207.9 L in 1 DRUM SOLUTION 207.9 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 29983-0017 ULTRA-SHIELD (CHLORHEXIDINE GLUCONATE) SOLUTION [IBA] 3 5 package rows 20250101_9f72719e-4650-4ec2-861b-e53545e0a630.zip
DailyMed Socrata Ingredients#