Home NDC 87414-0002 Bye Zero
Product NDC 87414-0002
11-digit product format 874140002
Labeler code 87414
Product ID 87414-0002_4a0e3f61-9668-eb5f-e063-6294a90a9a71
Type HUMAN OTC DRUG
Nonproprietary name Magnesium
Dosage form LIQUID
Route TOPICAL
Labeler Korea Life Science
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-10-06
Substance MAGNESIUM
Active strength 4.95 g/500mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Bye Zero
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM 4.95 g/500mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination I38ZP9992A Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87414-0002-1 Bye Zero 90 mL in 1 BOTTLE, SPRAY LIQUID 90 1
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87414-0002-1 87414000201 90 mL in 1 BOTTLE, SPRAY (87414-0002-1) 90 ml 2023-06-20 No No Current