Home NDC 81840-3333-2 NDC 81840-3333-2 - Hoo gargle (apple spearmint flavor) 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 81840-3333
Requested NDC 81840-3333-2
Package NDCs from labels 81840-3333-0, 81840-3333-1, 81840-3333-2, 81840-3333-3, 81840-3333-4, 81840-3333-5
Manufacturer MIKO CO LTD
Effective date 2023-10-06
Current FDA listing Not matched in FDA.report NDC product tables
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81840-3333-0 Hoo gargle (apple spearmint flavor) 10 mL in 1 POUCH LIQUID 10 4 81840-3333-1 Hoo gargle (apple spearmint flavor) 10 in 1 PACKAGE LIQUID 10 4 81840-3333-2 Hoo gargle (apple spearmint flavor) 15 in 1 PACKAGE LIQUID 15 4 81840-3333-3 Hoo gargle (apple spearmint flavor) 30 in 1 PACKAGE LIQUID 30 4 81840-3333-4 Hoo gargle (apple spearmint flavor) 50 in 1 PACKAGE LIQUID 50 4 81840-3333-5 Hoo gargle (apple spearmint flavor) 100 in 1 PACKAGE LIQUID 100 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81840-3333 HOO GARGLE (APPLE SPEARMINT FLAVOR) (SODIUM FLOURIDE) LIQUID [MIKO CO LTD] 4 Legacy NDC, 6 package rows 20231007_e9148945-57e6-2bba-e053-2995a90a8af3.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 60 of 60 · 1,181 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ionite H SODIUM FLUORIDE, POTASSIUM NITRATE Dharma Research, Inc. 642fec99-c5c5-4ef2-986e-5b5f7cf460de 2015-08-02 Warnings, Adverse reactions Exact identifier unii: 8ZYQ1474W7
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.