Home NDC 69164-0001 NDC 69164-0001 - COLLOIDAL IODINEINJECTION 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 69164-0001
Package NDCs from labels 69164-0001-1
Manufacturer JCI Colloidal Iodine Laboratory Co., Ltd.
Effective date 2023-05-17
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Drug Facts JCI Colloidal Iodine Laboratory Co., Ltd. 2023-05-17 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69164-0001-1 COLLOIDAL IODINEINJECTION 50 mL in 1 BOTTLE, GLASS SOLUTION 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69164-0001 COLLOIDAL IODINEINJECTION (IODINE) SOLUTION [JCI COLLOIDAL IODINE LABORATORY CO., LTD.] 1 1 package rows 20230519_fbf00a3a-e2c3-deb3-e053-6394a90abde7.zip