Home NDC 80762-0020 NDC 80762-0020 - Bye Zero 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 80762-0020
Package NDCs from labels 80762-0020-1
Manufacturer Korea Life Science
Effective date 2023-10-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Bye Zero - Korea Life Science Korea Life Science 2023-10-13 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80762-0020-1 Bye Zero 90 mL in 1 BOTTLE, SPRAY LIQUID 90 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80762-0020 BYE ZERO (MAGNESIUM) LIQUID [KOREA LIFE SCIENCE] 2 1 package rows 20231014_fe88e417-e671-da11-e053-6294a90ac0d2.zip