Home NDC 73489-005 NDC 73489-005 - ULTRA HIS MINT 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 73489-005
Package NDCs from labels 73489-005-01, 73489-005-02
Manufacturer CROWN GENERAL AGENCY INC
Effective date 2021-10-22
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73489-005-01 ULTRA HIS MINT 30 in 1 BOTTLE, PLASTIC CAPSULE 30 2 73489-005-02 ULTRA HIS MINT 60 in 1 BOTTLE, PLASTIC CAPSULE 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73489-005 ULTRA HIS MINT (GREEN TEA LEAF, ACETYLCARNITINE HYDROCHLORIDE, ARGININE HYDROCHLORIDE, N-MONOACETYLCYSTINE, TRIBULUS TERRESTRIS FRUIT, MARITIME PINE, UBIDECARENONE , LYCOPENE) CAPSULE [CROWN GENERAL AGENCY INC] 2 2 package rows 20211023_0fc229f3-d734-446a-a088-231585fb6807.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 131 of 131 · 2,601 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TiZO2 TITANIUM DIOXIDE, ZINC OXIDE Fallien Cosmeceuticals, LTD. 30468afc-9616-4765-b046-12e97a0a7827 2010-12-20 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.